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3-BROMO-5-CHLOROTOLUENE

CAS No.
329944-72-1
Chemical Name:
3-BROMO-5-CHLOROTOLUENE
Synonyms
3-bromo-5-chlorotlouene;3-BROMO-5-CHLOROTOLUENE;3-Bromo-5-chlorotoluene 98%;3-Chloro-5-methyl-bromobenzene;1-BROMO-3-CHLORO-5-METHYLBENZENE;Benzene,1-bromo-3-chloro-5-methyl-
CBNumber:
CB3442861
Molecular Formula:
C7H6BrCl
Molecular Weight:
205.48
MDL Number:
MFCD08437596
MOL File:
329944-72-1.mol
MSDS File:
SDS
Last updated:2025-08-08 17:45:00

3-BROMO-5-CHLOROTOLUENE Properties

Melting point 25℃
Boiling point 222.3±20.0℃ (760 Torr)
Density 1.535±0.06 g/cm3 (20 ºC 760 Torr)
Flash point 101.5±11.9℃
storage temp. Sealed in dry,Room Temperature
solubility Chloroform, Ethyl Acetate
form Solid
color Pale Yellow
InChI InChI=1S/C7H6BrCl/c1-5-2-6(8)4-7(9)3-5/h2-4H,1H3
InChIKey YRIKDGJWRMHTJP-UHFFFAOYSA-N
SMILES C1(Br)=CC(C)=CC(Cl)=C1

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P271-P280
Hazard Codes  Xi,Xn
Risk Statements  22
Hazard Note  Irritant
HS Code  2903998090

3-BROMO-5-CHLOROTOLUENE price More Price(26)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC B682490 3-Bromo-5-chlorotoluene 329944-72-1 10g $130 2021-12-16 Buy
TRC B682490 3-Bromo-5-chlorotoluene 329944-72-1 100g $375 2021-12-16 Buy
Biosynth Carbosynth FB140165 1-Bromo-3-chloro-5-methylbenzene 329944-72-1 100g $462 2021-12-16 Buy
American Custom Chemicals Corporation HCH0021313 3-BROMO-5-CHLORO TOLUENE 95.00% 329944-72-1 5G $864.27 2021-12-16 Buy
Medical Isotopes, Inc. 68224 3-Bromo-5-chlorotoluene 329944-72-1 100g $875 2021-12-16 Buy
Product number Packaging Price Buy
B682490 10g $130 Buy
B682490 100g $375 Buy
FB140165 100g $462 Buy
HCH0021313 5G $864.27 Buy
68224 100g $875 Buy

3-BROMO-5-CHLOROTOLUENE Chemical Properties,Uses,Production

Uses

3-Bromo-5-chlorotoluene is a reagent used in the synthesis of novel benzophenones towards the discovery of potent, next generation HIV nonnucleoside reverse transcriptase inhibitors.

Synthesis

2-Bromo-6-chloro-4-methylaniline

135340-78-2

3-BROMO-5-CHLOROTOLUENE

329944-72-1

2-Bromo-6-chloro-4-methylaniline (30 mmol) was used as a starting material, which was dissolved in a mixed solution of acetic acid (60 mL), water (25 mL), and concentrated hydrochloric acid (7 mL), and the reaction system was subsequently cooled to 5 °C. A solution of sodium nitrite (48 mmol, 3.31 g) in water (12 mL) was added slowly and dropwise while keeping the temperature below 5 °C. After the dropwise addition, the reaction mixture was continued to be stirred at 5-10 °C for 2 hours. Subsequently, the reaction solution was poured into a 50% hypophosphite solution pre-cooled to 0 °C and stirred for 48 h at room temperature. Upon completion of the reaction, extraction was carried out with dichloromethane (3 x 120 mL). The organic phases were combined, washed with saturated saline (100 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure to remove the solvent. Finally, the residue was purified by fast column chromatography to obtain the target product 3-bromo-5-chlorotoluene.

References

[1] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 22, p. 5568 - 5572
[2] Journal of Medicinal Chemistry, 2001, vol. 44, # 12, p. 1866 - 1882
[3] Journal of Medicinal Chemistry, 2001, vol. 44, # 12, p. 1866 - 1882

3-BROMO-5-CHLOROTOLUENE Preparation Products And Raw materials

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3-BROMO-5-CHLOROTOLUENE Spectrum

3-Bromo-5-chlorotoluene 98% 3-BROMO-5-CHLOROTOLUENE 1-BROMO-3-CHLORO-5-METHYLBENZENE 3-bromo-5-chlorotlouene 3-Chloro-5-methyl-bromobenzene Benzene,1-bromo-3-chloro-5-methyl- 329944-72-1 blocks Bromides