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4-(Butylsulfonyl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51770-72-0

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51770-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51770-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,7,7 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51770-72:
(7*5)+(6*1)+(5*7)+(4*7)+(3*0)+(2*7)+(1*2)=120
120 % 10 = 0
So 51770-72-0 is a valid CAS Registry Number.

51770-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(Butylsulfonyl)aniline

1.2 Other means of identification

Product number -
Other names 4-butylsulfonylaniline

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:51770-72-0 SDS

51770-72-0Relevant academic research and scientific papers

Photorefractive effect of liquid crystalline polymers possessing azobenzene chromophores

Sasaki, Takeo,Kai, Ryutaro,Sato, Atsushi,Ishikawa, Yuichi,Yoshimi, Takeshi

, p. 53 - 70 (2007/10/03)

A series of liquid crystalline polymers possessing azobenzene chromophores were synthesized, and in each polymer the photorefractive effect of the isotropic phase was investigated. The photorefractive effect was evaluated by a four-wave mixing experiment.

Syntheses of Some Alkyl-, Cycloalkyl-, and Aryl-(4-aminophenyl)-sulfones

Courtin, Alfred

, p. 1046 - 1052 (2007/10/02)

Syntheses of (4-aminophenyl)-alkyl, -cycloalkyl and -aryl sulfones 2 were achieved both by alkylation of 4-(acetylamino)-benzenesulfinic acid (7) to the corresponding acetanilides 9 followed by hydrolysis and by oxidation of the appropriate (4-nitrophenyl)-sulfides 11 to (4-nitrophenyl)-sulfones 1 with subsequent Bechamp reduction.

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