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37750-33-7

37750-33-7

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37750-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37750-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,5 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37750-33:
(7*3)+(6*7)+(5*7)+(4*5)+(3*0)+(2*3)+(1*3)=127
127 % 10 = 7
So 37750-33-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H10BrNS/c13-9-1-5-11(6-2-9)15-12-7-3-10(14)4-8-12/h1-8H,14H2

37750-33-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-bromophenyl)sulfanylaniline,hydrochloride

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:37750-33-7 SDS

37750-33-7Relevant articles and documents

Iodine/DMSO-Promoted Selective Direct Arylthiation of Anilines with Thiols under Metal-Free Conditions

Zhao, Wenqi,Zhang, Feng,Deng, Guo-Jun

, p. 291 - 301 (2021/01/14)

An iodine-promoted divergent thiolation of unprotected anilines with thiols for the synthesis of sulfide anilines has been described. The combinational use of I2 and DMSO played an important role to realize this kind of transformation without the aid of a

Synthesis of molecular chains: phenylene thioether and sulfoxide oligomers

Vicente, José,Abad, José A.,López-Nicolás, Rosa M.

, p. 6281 - 6288 (2008/09/21)

The application of a general synthetic approach to prepare molecular chains is reported. It is based on a step-by-step method each consisting first in a Pd-catalyzed reaction between ArI and HXAr′Br (Ar=aryl, Ar′=arylene) to give ArXAr′Br followed by a Cu

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