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Cyclopropyl bromide

CAS No.
4333-56-6
Chemical Name:
Cyclopropyl bromide
Synonyms
BROMOCYCLOPROPANE;Cyclopropyl;Cyclopropyl bromine;BromocycL;NSC 89692;bromo-cyclopropan;1-Bromocyclopropane;CYCLOPROPYL BROMIDE;Cyclopropane, bromo-;Bromocyclopropane>
CBNumber:
CB8421267
Molecular Formula:
C3H5Br
Molecular Weight:
120.98
MDL Number:
MFCD00001271
MOL File:
4333-56-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 05:12:12
Product description Number Pack Size Price
Bromocyclopropane 99% C117307 5g $87.7
Bromocyclopropane 99% C117307 25g $187
Bromocyclopropane >98.0%(GC) C1067 5g $50
Bromocyclopropane >98.0%(GC) C1067 25g $145
Bromocyclopropane TRC-B682760-5G 5g $72
More product size

Cyclopropyl bromide Properties

Boiling point 69 °C (lit.)
Density 1.51 g/mL at 25 °C (lit.)
refractive index n20/D 1.458(lit.)
Flash point 20 °F
storage temp. 2-8°C
solubility Chloroform (Sparingly), Methanol (Slightly)
form Liquid
Specific Gravity 1.510
color Clear colorless
Water Solubility immiscible
BRN 1900287
InChI InChI=1S/C3H5Br/c4-3-1-2-3/h3H,1-2H2
InChIKey LKXYJYDRLBPHRS-UHFFFAOYSA-N
SMILES C1(Br)CC1
CAS DataBase Reference 4333-56-6(CAS DataBase Reference)
NIST Chemistry Reference Cyclopropyl bromide(4333-56-6)
EPA Substance Registry System Cyclopropane, bromo- (4333-56-6)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Flame (GHS02)
GHS02
Signal word  Danger
Hazard statements  H225
Precautionary statements  P210-P233-P240-P241-P242-P243
PPE Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes  F,Xi
Risk Statements  11-36/37/38
Safety Statements  16-26-36-37/39
RIDADR  UN 1993 3/PG 2
WGK Germany  3
8-19
Hazard Note  Irritant
TSCA  TSCA listed
HazardClass  3
PackingGroup  II
HS Code  29035990
Storage Class 3 - Flammable liquids
Hazard Classifications Flam. Liq. 2
Limited Quantities 1.0 L (0.3 gallon) (liquid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
NFPA 704
4
2 0

Cyclopropyl bromide price More Price(74)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich C117307 Bromocyclopropane 99% 4333-56-6 5g $87.7 2026-04-30 Buy
Sigma-Aldrich C117307 Bromocyclopropane 99% 4333-56-6 25g $187 2026-04-30 Buy
TCI Chemical C1067 Bromocyclopropane >98.0%(GC) 4333-56-6 5g $50 2026-04-30 Buy
TCI Chemical C1067 Bromocyclopropane >98.0%(GC) 4333-56-6 25g $145 2026-04-30 Buy
TRC TRC-B682760-5G Bromocyclopropane 4333-56-6 5g $72 2026-06-03 Buy
Product number Packaging Price Buy
C117307 5g $87.7 Buy
C117307 25g $187 Buy
C1067 5g $50 Buy
C1067 25g $145 Buy
TRC-B682760-5G 5g $72 Buy

Cyclopropyl bromide Chemical Properties,Uses,Production

Description

Cyclopropyl bromide is also named as Bromocyclopropane. It is used in organic synthesis, for instance, for the formation of a Grignard Reagent, cyclopropyllithium. It is also used as an intermediate in the manufacture of pharmaceutical and agrochemical products.

Chemical Properties

Light yellow to clear colourless liquid, boiling point 67-69°C, refractive index (nD20) 1.4605, density (d420) 1.5120, flash point -6°C.

Uses

Bromocyclopropane is primarily used an intermediate in the manufacture of pharmaceutical and agrochemical products. It is also used in the production of cyclopropyl boric acid. It is used as an intermediate in organic synethesis.

Application

Bromocyclopropane have anti-angiogenic effects that inhibits the growth of new blood vessels by interfering with the production of prostaglandins and nitric oxide, which are important for the formation of new blood vessels. Bromocyclopropane binds to cyclopropyl and hydrochloric acid, forming a hydrogen bond. It also forms a hydrogen bond with fatty acids and an a-type hydroxyl group.

Preparation

Bromocyclopropane has been prepared by the Hunsdiecker reaction by adding silver cyclopropanecarboxylate to bromine in dichlorodifluoromethane at 29° (53% yield) or in tetrachloroethane at 20° to 25° (15–20% yield). Decomposition of the peroxide of cyclopropanecarboxylic acid in the presence of carbon tetrabromide gave bromocyclopropane in 43% yield. An attempt to prepare the bromide via the von Braun reaction was unsuccessful. Ten percent yields are reported for the photobromination of cyclopropane and the photochemical rearrangement of allyl bromide. Treatment of 1,1,3-tribromopropane with methyllithium prepared from methyl bromide furnishes a 60–65% yield of bromocyclopropane.

Synthesis

Cyclopropanecarboxylic acid

1759-53-1

Cyclopropyl bromide

4333-56-6

(1) 179 g of 1,3-bromochloropropane was added to a three-necked flask, 29 g of potassium cyanide and 50 ml of water were added and heated and stirred until completely dissolved. Subsequently, 70 ml of ethanol solution was added and the mixture was stirred and refluxed for 2 hours. After completion of the reaction, it was cooled to room temperature and diluted with 300 ml of water to separate the oil and aqueous phases. The aqueous phase was extracted with 40 ml of chloroform, the organic phases were combined and dried with anhydrous calcium chloride. 316.9 g of hydrogen chloride was obtained. Chlorobutanenitrile 241.6 g was prepared by adding 100 ml of sodium hydroxide solution and stirring the reaction for 2 hours. Then 200 ml of water was added, cooled to about 10°C, 44 ml of concentrated sulfuric acid was added to acidify the reaction mixture, extracted with petroleum ether as an extractant, the organic phases were combined and dried with anhydrous sodium sulfate to obtain 330.1 g of cyclopropionic acid. (2) 324.8 g of cyclopropionic acid was added dropwise to a reaction flask with 48 g of mercuric oxide, 160 ml of a mixture of 1,1,2,2-tetrachloroethane and 64.4 g of liquid bromine, and stirred for 2 hours. After completion of the reaction, the mixture was cooled to 5°C, washed with tetrachloroethane and then dried with calcium chloride to give 419.15 g of bromocyclopropane.

References

Science of Synthesis: Houben-Weyl Methods of Molecular Transformation Vol. 7: Compounds of Group 13 and 2 (Al, Ga, In, Tl, Be…Ba), 2007, ISBN: 9783131484819
D. Seyferth, H. M. Cohen, The Stability of Cyclopropyllithium in diethyl ether and in tetrahydrofuran, Journal of Organometallic Chemistry, 1963, vol. 1, pp. 15-21
“Formal Nucleophilic Substitution of Bromocyclopropanes with Azoles”, Ryabchuk, P.; Rubina, M.; Xu, J.; Rubin, M. Org. Lett. 2012, 14, 1752.
“Formal Substitution of Bromocyclopropanes with Nitrogen Nucleophiles”, Banning, J. E.; Gentillon, J.; Ryabchuk, P. G.; Prosser, A. R.; Rogers, A.; Edwards, A.; Holtzen, A.; Babkov, I.; Rubina, M.; Rubin, M. J. Org. Chem., 2013, 78, 7601.

1759-53-1
4333-56-6
Synthesis of Cyclopropyl bromide from Cyclopropanecarboxylic acid
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View Lastest Price from Cyclopropyl bromide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
 Cyclopropyl bromide pictures 2026-05-28 Cyclopropyl bromide
4333-56-6
$200.60 1KG 99% 5000kg Hebei Chuanghai Biotechnology Co,.LTD
Cyclopropyl bromide pictures 2025-09-25 Cyclopropyl bromide
4333-56-6
$1.00-100.00 1KG 99% Henan Fengda Chemical Co., Ltd
Bromocyclopropane pictures 2025-09-12 Bromocyclopropane
4333-56-6
$860.00 99 % 5000 Kg R&D Scientific Inc.
bromo-cyclopropan Cyclopropane, bromo- CYCLOPROPYL BROMIDE Cyclopropylbromide,99% Bromocyclopropane,99% Cyclopropyl bromide(CPB) CYCLOPROPYL BROMIDE, 98%CYCLOPROPYL BROMIDE, 98%CYCLOPROPYL BROMIDE, 98%CYCLOPROPYL BROMIDE, 98% BromocycL 1-Bromocyclopropane Cyclopropyl Bromide / Bromocyclopropane (CPB) Cyclopropyl bromide ,98.5% Bromocyclopropane,Cyclopropyl bromide NSC 89692 BROMOCYCLOPROPANE FOR SYNTHESIS BroMocyclopropane, 98.5% Bromocyclopropane> Cyclopropyl bromide ISO 9001:2015 REACH Brominated cyclopropane Bromo Cyclopropane( GRAMS) Cyclopropyl Bromide / Bromo cyclopropane Bromocyclopropane, 98% Cyclopropane bromide BROMOCYCLOPROPANE Cyclopropyl Cyclopropyl bromine 4333-56-6 C3H5Br HALOGEN Simple 3-Membered Ring Compounds Cyclopropanes Building Blocks Alkyl Organic Building Blocks Halogenated Hydrocarbons Pyridines Alkyl Building Blocks Chemical Synthesis Halogenated Hydrocarbons Organic Building Blocks Miscellaneous Reagents Pharmaceutical Intermediates Cyclopropanes Simple 3-Membered Ring Compounds 4333-56-6