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Benzamide, N-[[[2-(1-methylethenyl)phenyl]amino]thioxomethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88884-37-1

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88884-37-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88884-37-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,8,8 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88884-37:
(7*8)+(6*8)+(5*8)+(4*8)+(3*4)+(2*3)+(1*7)=201
201 % 10 = 1
So 88884-37-1 is a valid CAS Registry Number.

88884-37-1SDS

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 N-[(2-prop-1-en-2-ylphenyl)carbamothioyl]benzamide

1.2 Other means of identification

Product number -
Other names Benzamide,N-[[[2-(1-methylethenyl)phenyl]amino]thioxomethyl]

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:88884-37-1 SDS

88884-37-1Downstream Products

88884-37-1Relevant academic research and scientific papers

A Versatile Synthesis of Functionalised 2-Aminoquinolines by Mercury Controlled Cyclisation of 2-Vinylphenylthioureas

Wiggall, Kenneth J.,Richardson, Stewart K.

, p. 867 - 870 (2007/10/02)

4-(4-Hydroxyphenyl)-2-phenylamino-1,8-naphthyridine was prepared via cyclization of N-phenyl-N'-3-(4-hydroxyphenethen-1-yl)pyridin-2-ylthiourea in the presence of mercuric oxide.Derivatives of 4-methyl-2-aminoquinolines were prepared in a similar manner f

Improved Procedures for the Preparation of Cycloalkyl-, Arylalkyl-, and Arylthioureas

Rasmussen, C. R.,Villani, F. J.,Weaner, L. E.,Reynolds, B. E.,Hood, A. R.,et al.

, p. 456 - 459 (2007/10/02)

An improved procedure for the preparation of arylthioureas consists of the reaction of benzoyl isothiocyanate with anilines in acetone and debenzoylation of the resultant N-aryl-N'-benzoylthioureas with 5percent aqueous sodium hydroxide.Bicycloalkylthioureas and N-(arylalkyl)thioureas (e.g. 9H-9-fluorenylthiourea) are directly prepared from the corresponding isothiocyanates and ammonia.

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