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Benzyl 2-bromoacetate

CAS No.
5437-45-6
Chemical Name:
Benzyl 2-bromoacetate
Synonyms
BENZYL BROMOACETATE;merbac35;TIMTEC-BB SBB006752;BENZYL 2-BROMOACETATE;Benzyl a-Bromoacetate;BroMine benzyl acetate;Benzylbromoacetate,97%;Benzyl broMoacetate 96%;Bromoacetic acid benzyl;Benzyl Bromoacetate >
CBNumber:
CB9413740
Molecular Formula:
C9H9BrO2
Molecular Weight:
229.07
MDL Number:
MFCD00000190
MOL File:
5437-45-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 06:19:54
Product description Number Pack Size Price
Benzyl bromoacetate 96% 245631 50g $44.8
Benzyl bromoacetate 96% 245631 250g $149
Benzyl Bromoacetate >96.0%(GC) B1674 25g $22
Benzyl Bromoacetate >96.0%(GC) B1674 500g $196
Benzyl 2-bromoacetate 209148 250.00g $123
More product size

Benzyl 2-bromoacetate Properties

Melting point 199-201 °C(Solv: water (7732-18-5))
Boiling point 166-170 °C22 mm Hg(lit.)
Density 1.446 g/mL at 25 °C(lit.)
refractive index n20/D 1.544(lit.)
Flash point >230 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform, Methanol
form Liquid
Specific Gravity 1.446
color Clear colorless to light yellow
Water Solubility Not miscible or difficult to mix in water.
BRN 973658
InChI 1S/C9H9BrO2/c10-6-9(11)12-7-8-4-2-1-3-5-8/h1-5H,6-7H2
InChIKey JHVLLYQQQYIWKX-UHFFFAOYSA-N
SMILES BrCC(=O)OCc1ccccc1
LogP 2.368 (est)
CAS DataBase Reference 5437-45-6(CAS DataBase Reference)
Indirect Additives used in Food Contact Substances BENZYL BROMOACETATE
FDA 21 CFR 175.105
EWG's Food Scores 1
FDA UNII 64U2RK18D3
NIST Chemistry Reference Benzyl 2-bromoacetate(5437-45-6)
EPA Substance Registry System Benzyl bromoacetate (5437-45-6)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
target organs Respiratory system
PPE Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-37/39
RIDADR  2810
WGK Germany  3
RTECS  AF5957215
19
HS Code  29159080
Storage Class 10 - Combustible liquids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
REACH Registrations Active
NFPA 704
1
2 0

Benzyl 2-bromoacetate price More Price(49)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 245631 Benzyl bromoacetate 96% 5437-45-6 50g $44.8 2026-04-30 Buy
Sigma-Aldrich 245631 Benzyl bromoacetate 96% 5437-45-6 250g $149 2026-04-30 Buy
TCI Chemical B1674 Benzyl Bromoacetate >96.0%(GC) 5437-45-6 25g $22 2026-04-30 Buy
TCI Chemical B1674 Benzyl Bromoacetate >96.0%(GC) 5437-45-6 500g $196 2026-04-30 Buy
Matrix Scientific 209148 Benzyl 2-bromoacetate 5437-45-6 250.00g $123 2026-05-18 Buy
Product number Packaging Price Buy
245631 50g $44.8 Buy
245631 250g $149 Buy
B1674 25g $22 Buy
B1674 500g $196 Buy
209148 250.00g $123 Buy

Benzyl 2-bromoacetate Chemical Properties,Uses,Production

Chemical Properties

Colorless to light yellow liqui

Uses

It is employed in biological research purpose. Benzyl bromoacetate was used in the alkylation of (-)-2,3-O-isopropylidene-D-threitol that afforded lipopeptide, 2-[(4R,5R)-5-({[(9H-fluoren-9-yl)methoxy]carbonylaminomethyl}-2,2-dimethyl-1,3-dioxolan-4-yl)methoxy]acetic acid.

Synthesis

Bromoacetic acid

79-08-3

Benzyl alcohol

100-51-6

Benzyl ether

103-50-4

Benzyl 2-bromoacetate

5437-45-6

General method: A mixture of acid 2 (0.033 g), 2-bromoacetic acid (3a) (0.137 g, 0.988 mmol) adsorbed on silica gel and benzyl alcohol (4a) (0.108 g, 1.000 mmol) was stirred and reacted at 80°C for 24 h under argon protection. After completion of the reaction, the mixture was cooled to room temperature, ether (5 mL x 5) was added for extraction, and the organic layer was separated by decantation from the silica gel adsorbed acid 2. The organic layer was concentrated under reduced pressure to remove the solvent, and then purified by silica gel column chromatography to afford benzyl 2-bromoacetate (5aa) (0.189 g, 83% yield) using hexane/ethyl acetate (v/v = 10/1) as eluent. The silica gel adsorbed acid 2 was recovered by vacuum drying at room temperature to give a white powder (0.033 g, 99% recovery).

Purification Methods

Dilute the ester with Et2O, wash it with 10% aqueous NaHCO3, H2O, dry (MgSO4) and fractionate it using a Fenske (glass helices packing) column. [Bergmann & Szinai J Chem Soc 1521 1956, Beilstein 6 IV 2265.] LACHRYMATORY.

References

[1] Journal of Molecular Catalysis A: Chemical, 2013, vol. 367, p. 116 - 120

79-08-3
100-51-6
5437-45-6
Synthesis of Benzyl 2-bromoacetate from Bromoacetic acid and Benzyl alcohol
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View Lastest Price from Benzyl 2-bromoacetate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
benzyl bromoacetate pictures 2025-09-25 benzyl bromoacetate
5437-45-6
US $8.00-0.80 / KG 1KG 99% g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
Benzyl 2-bromoacetate pictures 2025-04-04 Benzyl 2-bromoacetate
5437-45-6
US $0.00-0.00 / kg 1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
Benzyl 2-bromoacetate pictures 2021-07-13 Benzyl 2-bromoacetate
5437-45-6
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
bromo-aceticacibenzylester bromo-aceticaciphenylmethylester acetic acid (phenylmethyl)bromanuidyl ester Benzyl 2-broMoacetate, 96% 50GR Bromoacetic acid benzyl ester, Benzyl bromoethanoate BroMine benzyl acetate 2-Bromoacetic Acid Phenylmethyl Ester Benzyl broMoacetate 96% TIMTEC-BB SBB006752 merbac35 BROMOACETIC ACID BENZYL ESTER BENZYL BROMOACETATE BENZYL 2-BROMOACETATE 2-BROMO-ACETIC ACID BENZYLESTER Benzyl-2-Bromoacetate96% Benzylbromoacetate,97% Acetic acid, bromo-, benzyl ester Acetic acid, bromo-, phenylmethyl ester Benzyl a-Bromoacetate bromo-acetic acid phenylmethyl ester Bromoacetic acid benzyl este Phenylmethyl 2-bromoacetate Bromoacetic acid benzyl 1-Bromo-3-oxa-4-phenylbutan-2-one Benzyl 2-broMoacetate, 96% 250GR Benzyl Bromoacetate > Acetic acid, 2-bromo-, phenylmethyl ester BENZYL 2-BROMOACETATE CAS 5437-45-6 5437-45-6 BrCH2COOCH2C6H5 C6H5CH2CO2CH2Br HALOGEN Carbonyl Compounds C8 to C9 Building Blocks Organic Building Blocks Esters Building Blocks C8 to C9 Carbonyl Compounds Chemical Synthesis Esters Organic Building Blocks Pharmaceutical Intermediates