ChemicalBook--->CAS DataBase List--->867366-91-4

867366-91-4

867366-91-4 Structure

867366-91-4 Structure
IdentificationBack Directory
[Name]

3-BROMO-5-METHOXY BENZONITRILE
[CAS]

867366-91-4
[Synonyms]

3-Bromo-5-cyanoanisole
3-BROMO-5-METHOXYBENZOTRILE
3-BROMO-5-METHOXY BENZONITRILE
Benzonitrile, 3-bromo-5-methoxy-
3-BROMO-5-METHOXYBENZONITRILE,98%
3-Bromo-5-methoxybenzonitrile 99%
3-Bromo-5-cyanoanisole, 5-Bromo-m-anisonitrile
[Molecular Formula]

C8H6BrNO
[MDL Number]

MFCD08061971
[MOL File]

867366-91-4.mol
[Molecular Weight]

212.04
Chemical PropertiesBack Directory
[Boiling point ]

253.5±25.0 °C(Predicted)
[density ]

1.56±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[form ]

crystalline solid
[color ]

White
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332
[Precautionary statements ]

P280
[RIDADR ]

UN3439
[HazardClass ]

6.1
[HS Code ]

2926907090
Spectrum DetailBack Directory
[Spectrum Detail]

3-BROMO-5-METHOXY BENZONITRILE(867366-91-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

Benzaldehyde, 3-bromo-5-methoxy-, oxime

867366-90-3

3-BROMO-5-METHOXY BENZONITRILE

867366-91-4

The general procedure for the synthesis of 3-bromo-5-methoxybenzonitrile from the compound (CAS:867366-90-3) is as follows: a mixed solution of aldehyde 180b (12.0 g, 56 mmol), hydroxylamine hydrochloride (19.4 g, 5 eq.), ethanol (100 mL), and pyridine (10 mL) was heated to 65 °C and reacted for 16 hours. After completion of the reaction, the mixture was cooled to room temperature and extracted by partitioning with 50% ethyl acetate/hexane and water. The organic layer was washed with brine and dried with magnesium sulfate. After evaporation of the volatiles, 12.4 g of the oxime product was obtained (97% yield). The resulting oxime was dissolved in anhydrous dioxane (100 mL) and pyridine (26 mL, 6 eq.), the solution was cooled to 0 °C and trifluoroacetic anhydride (15 mL, 2 eq.) was added slowly. Subsequently, the mixture was gradually warmed to room temperature and stirred continuously for 2 days. After that, the reaction solution was heated to 60 °C and kept for 1 hour. After completion of the reaction, the mixture was cooled to room temperature and carefully poured into ice water. The mixture was extracted with dichloromethane and the combined organic layers were washed sequentially with water, 1 M hydrochloric acid and brine. The organic layer was dried over magnesium sulfate and the solvent was evaporated to give the target product 180c 10.4 g (90% yield).

[References]

[1] Patent: US2005/239881, 2005, A1. Location in patent: Page/Page column 47-48
[2] Patent: US2008/20981, 2008, A1. Location in patent: Page/Page column 19
[3] Patent: US2008/45511, 2008, A1. Location in patent: Page/Page column 21
[4] Patent: US2008/293664, 2008, A1. Location in patent: Page/Page column 16
[5] Patent: US2008/249151, 2008, A1. Location in patent: Page/Page column 21
867366-91-4 suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Telephone: 18210857532 18210857532
Website: https://www.jkchemical.com
Company Name: Capot Chemical Co., Ltd  
Telephone: +86 (0) 571 85 58 67 18
Website: www.capotchem.com
Company Name: Shanghai Longsheng chemical Co.,Ltd.  
Telephone: 58099637 13585536065
Website: www.shlshg.com
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Telephone: 021-54306202 13764082696
Website: https://www.hanhongsci.com
Company Name: Wuhan ariel chemical Co., LTD.  
Telephone: 18986259541 18986259541
Website: http://www.3stc.com
Company Name: Shanghai Topbiochem Technology Co., Ltd  
Telephone: +86-21-60341587
Website: www.topbiochem.com
Company Name: Nanjing Norris-Pharm Technology Co., Ltd  
Telephone: 13901585132
Website:
Company Name: Shanghai Jian Chao Chemical Technology Co., Ltd.  
Telephone: 150-2103-5486 18017383231
Website:
Company Name: Shanghai Witofly Chemical Co.,Ltd  
Telephone:
Website: www.witofly.com
Company Name: Shanghai Raise Chemical Technology Co.,Ltd  
Telephone: +86-021-50935922
Website: www.raise-chem.com
Company Name: Shanghai Huikai Chemical Technology Co., Ltd.  
Telephone: 021-61995394 18916691159
Website: www.chemicalsea.com
Company Name: Nanjing ShengSai Chemical Co., Ltd.  
Telephone: 025-85205967 13951876367
Website: http://www.shengsaichem.com
Company Name: Bide Pharmatech Ltd.  
Telephone: 400-164-7117 18317119277
Website: www.bidepharm.com
Company Name: Mashilabs (Shanghai) Co.,Ltd.  
Telephone: 19916721580
Website: www.chemicalbook.com/ShowSupplierProductsList16374/0_EN.htm
Company Name: Tianjin Anhao Biological Technology Co., Ltd.  
Telephone:
Website: www.glsyntech.com
Company Name: Shanghai Yongye Biotechnology Co., Ltd.  
Telephone: 86-021-61559134 15921386130
Website: www.shyongye.com
Company Name: Shanghai Na Qian Chemical Technology Co. Ltd.  
Telephone: 13598610367 13598610367
Website: https://www.chemicalbook.com/supplier/11167012/
Company Name: Shanghai Jovan Biochemical Technology Co. Ltd.  
Telephone: +86-021-61654350
Website: www.chemicalbook.com/ShowSupplierProductsList16421/0_EN.htm
Tags:867366-91-4 Related Product Information