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2-bromotetralin

CAS No.
6134-56-1
Chemical Name:
2-bromotetralin
Synonyms
6-Bromotetralin;2-bromotetralin;Naphthalene, 6-bromo-1,2,3,4-tetrahydro-
CBNumber:
CB61570391
Molecular Formula:
C10H11Br
Molecular Weight:
211.1
MDL Number:
MFCD09842497
MOL File:
6134-56-1.mol
MSDS File:
SDS
Last updated:2026-05-28 03:58:12

2-bromotetralin Properties

Boiling point 241 °C
Density 1.384±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
Appearance Colorless to light yellow Liquid

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H319-H335-H302-H315
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501

2-bromotetralin price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich T263664 6-BROMO-1,2,3,4-TETRAHYDRONAPHTHALENE AldrichCPR 6134-56-1 5MG $121 2026-04-30 Buy
Activate Scientific AS7832 6-Bromo-1,2,3,4-tetrahydronaphthalene 95% 6134-56-1 1g $109 2026-06-04 Buy
Activate Scientific AS7832 6-Bromo-1,2,3,4-tetrahydronaphthalene 95% 6134-56-1 5g $391 2026-06-04 Buy
Matrix Scientific 202554 6-Bromotetralin 6134-56-1 1.00g $89 2026-05-18 Buy
Matrix Scientific 202554 6-Bromotetralin 6134-56-1 5.00g $355 2026-05-18 Buy
Product number Packaging Price Buy
T263664 5MG $121 Buy
AS7832 1g $109 Buy
AS7832 5g $391 Buy
202554 1.00g $89 Buy
202554 5.00g $355 Buy

2-bromotetralin Chemical Properties, Uses, Production

Synthesis

3-(4-BROMOBENZOYL)PROPIONIC ACID

6340-79-0

2-bromotetralin

6134-56-1

General procedure for the synthesis of 6-bromo-1,2,3,4-tetrahydro-naphthalene from 3-(4-bromobenzoyl)propionic acid: Freshly distilled chloroform (0.6 mL) was added to a screw-capped vial fitted with a magnetic stirring bar under the protection of nitrogen, and In(OAc)3 (0.0060 mmol, 1.8 mg), I2 (0.600 mmol, 152 mg), 3 -(4-bromobenzoyl)propionic acid (0.6 mmol) and Me2PhSiH (3.90 mmol, 600 μL). The vial was sealed with a cap with a PTFE septum. The reaction vial was heated in an oil bath and the progress of the reaction was monitored by gas chromatography (GC) and thin layer chromatography (TLC) until the carboxylic acid was completely consumed. Upon completion of the reaction, the mixture was cooled to room temperature and the reaction was quenched with 2 mL of aqueous HCl. The aqueous layer was extracted with hexane (5 mL × 3). The organic phases were combined, dried with anhydrous Na2SO4, and the solvent was evaporated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: hexane) to afford the target product 6-bromo-1,2,3,4-tetrahydro-naphthalene. If necessary, the product can be further purified by gel permeation chromatography (eluent: CHCl3).

References

[1] Chemistry Letters, 2015, vol. 44, # 11, p. 1503 - 1505

2-bromotetralin Suppliers

Global Suppliers ( 42)
Supplier Tel Email Country ProdList Advantage
Taizhou Tongxin Bio-Tech Co., Ltd 0523-86818997 18652728585 sales@allyrise.com China 2987 60
LABTER PHARMATECH(BEIJING) CO.,LTD 010-56330744 18310155299 sales@labter.com.cn China 19999 55
Shanghai YuanYe Biotechnology Co., Ltd. 15026964105 2881489226@qq.com China 89667 60
Amadis Chemical Company Limited 571-89925085 sales@amadischem.com China 131885 58
Yantai ShengKailun Chemical Technology Co., Ltd. 13356901049 3119594100@qq.com China 7964 55
Shanghai CR Corporation Limited 13917420128 13062833949 fred.wen@crcorporation.cn China 9776 58
Hangzhou Molcore Biopharmatech Co.,Ltd 400-711-5280 86-571-81025280 sales@molcore.com China 9957 58
Aikon International Limited 025-58851090 13913916777 sales01@aikonchem.com China 15947 58
Shanghai Jizhi Biochemical Technology Co. Ltd. 021-4009004166/18616739031 18616739031 3007523370@qq.com China 40000 58
Shanghai Huaxinwei Chemical Technology Co., Ltd. 18019176997 18019176997 zym19@126.com China 390 58

2-bromotetralin Spectrum

2-bromotetralin 6-Bromotetralin Naphthalene, 6-bromo-1,2,3,4-tetrahydro- 6134-56-1