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101-57-5

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101-57-5 Usage

General Description

4-Anilinobenzenesulfonic acid consists of a benzene ring with an amino group (-NH2) and a sulfonic acid group (-SO3H) attached to the 4-position, making it a member of the sulfonic acid family. 4-Anilinobenzenesulfonic acid is commonly used in the chemical industry as a precursor in the synthesis of various dyes and pigments.

Check Digit Verification of cas no

The CAS Registry Mumber 101-57-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 101-57:
(5*1)+(4*0)+(3*1)+(2*5)+(1*7)=25
25 % 10 = 5
So 101-57-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO3S/c14-17(15,16)12-8-6-11(7-9-12)13-10-4-2-1-3-5-10/h1-9,13H,(H,14,15,16)

101-57-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-anilinobenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names 4-(phenylamino)benzenesulphonic acid

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:101-57-5 SDS

101-57-5Relevant articles and documents

Fe-MIL-101 modified by isatin-Schiff-base-Co: a heterogeneous catalyst for C-C, C-O, C-N, and C-P cross coupling reactions

Farrokhi, Alireza,Rouzifar, Majid,Sansano, José Miguel,Sobhani, Sara

, p. 19963 - 19976 (2021/11/12)

A metal-organic framework functionalized with a cobalt-complex is preparedviapost-synthetic modification of Fe-MIL-101-NH2. Initially, Fe-MIL-101-NH2reacted with isatin to produce Fe-MIL-101-isatin-Schiff-base, which can anchor the cobalt by the addition of cobalt acetate. The resulting MOF-Co catalyst is characterized by employing multiple techniques. This new modified MOF acts as a heterogeneous and recyclable catalyst for efficient Ullmann, Buchwald-Hartwig, Hirao, Hiyama and Mizoroki-Heck cross-coupling reactions of several aryl halides/phenylboronic acid/phenyltosylate with phenols, anilines/heterocyclic amines, triethyl phosphite, triethoxyphenylsilane and alkenes and generates the expected coupling products in good to high yields.

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