ChemicalBook > Product Catalog >Pharmaceutical intermediates >Heterocyclic compound >Indole Compounds >6-bromoisoindolin-1-one

6-bromoisoindolin-1-one

6-bromoisoindolin-1-one Suppliers list
Company Name: Shanghai Yaochong Chemical Technology Co., Ltd  Gold
Tel: 13390851206
Email:
Company Name: Zhongshan Jukemei Biotechnology Co., Ltd.  Gold
Tel: 13642727863
Email: 1009049100@qq.com
Company Name: QINGDAO CARELONGPHARMATECH CO.,LTD  Gold
Tel: 053288191853 13061484198
Email: sales@carelongchem.com
Company Name: Shanghai Boyle Chemical Co., Ltd.  
Tel:
Email: sales@boylechem.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com

6-bromoisoindolin-1-one manufacturers

6-bromoisoindolin-1-one Basic information
Product Name:6-bromoisoindolin-1-one
Synonyms:6-Bromo-2,3-dihydroisoindolin-1-one;1H-Isoindol-1-one, 6-broMo-2,3-dihydro-;6-bromoisoindolin-1-one;6-broMo-2,3-dihydro-1H-isoindol-1-one;6-BroMo-2,3-dihydro-isoindol-1-one;6-BroMoisoindolin-1-one, 95+%;1-Piperidinecarboxylicacid,4-(2-bromoethyl)-,1,4-dimethylethylester;6-bromoisoindoleline-1-one
CAS:675109-26-9
MF:C8H6BrNO
MW:212.04
EINECS:
Product Categories:
Mol File:675109-26-9.mol
6-bromoisoindolin-1-one Structure
6-bromoisoindolin-1-one Chemical Properties
Boiling point 431.7±45.0 °C(Predicted)
density 1.666±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka13.87±0.20(Predicted)
form solid
color White to off-white
InChIInChI=1S/C8H6BrNO/c9-6-2-1-5-4-10-8(11)7(5)3-6/h1-3H,4H2,(H,10,11)
InChIKeyHYTCKZQYVIURAW-UHFFFAOYSA-N
SMILESC1(=O)C2=C(C=CC(Br)=C2)CN1
Safety Information
HS Code 2925199590
MSDS Information
6-bromoisoindolin-1-one Usage And Synthesis
Synthesis
5-BROMO-2-BROMOMETHYL-BENZOIC ACID METHYL ESTER

79670-17-0

6-bromoisoindolin-1-one

675109-26-9

The general procedure for the synthesis of 6-bromoisoindolin-1-one from 5-bromo-2-bromomethylbenzoic acid methyl ester was as follows: gentle bubbling of ammonia into a 1:1 THF/MeOH mixture of 5-bromo-2-bromomethylbenzoic acid methyl ester (1 eq.) was carried out for 40 min at room temperature. Upon completion of the reaction, the reaction mixture was concentrated under vacuum. The concentrated residue was sonicated in CH2Cl2 for 15 min followed by filtration to afford the target product 6-bromo-2,3-dihydro-isoindol-1-one as a white solid (98% yield, 90% purity). Product mass spectral data: m/z (LC-MS, ESP): 212.3/214.3 [M + H]+, retention time R/T = 2.98 min.

References[1] Patent: WO2008/23161, 2008, A1. Location in patent: Page/Page column 117
[2] Organic and Biomolecular Chemistry, 2017, vol. 15, # 48, p. 10172 - 10183
[3] Patent: CN107474006, 2017, A. Location in patent: Paragraph 0050; 0051; 0054; 0056-0057; 0060; 0062-0063; 0066
[4] Patent: WO2008/20306, 2008, A2. Location in patent: Page/Page column 38
[5] E-Journal of Chemistry, 2011, vol. 8, # 3, p. 1108 - 1113
Tag:6-bromoisoindolin-1-one(675109-26-9) Related Product Information
4-bromoisoindolin-1-one 4-nitroisoindolin-1-one 6-AMino-2,3-dihydroisoindol-1-one 6-Nitro-isoindolin-1-one 5-Bromo-2,3-dihydro-isoindol-1-one 4-Bromophthalimide