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Methanesulfenamide, N-(phenylmethylene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61076-36-6

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61076-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61076-36-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,7 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61076-36:
(7*6)+(6*1)+(5*0)+(4*7)+(3*6)+(2*3)+(1*6)=106
106 % 10 = 6
So 61076-36-6 is a valid CAS Registry Number.

61076-36-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methylsulfanyl-1-phenylmethanimine

1.2 Other means of identification

Product number -
Other names Methanesulfenamide,N-(phenylmethylene)

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:61076-36-6 SDS

61076-36-6Downstream Products

61076-36-6Relevant academic research and scientific papers

Method for synthesizing N - sulfur-based benzimide or derivative thereof from Bununte salt (by machine translation)

-

Paragraph 0045-0049; 0076-0091, (2019/09/13)

The Bununte salt is used for synthesizing N - thienylbenzimide or a derivative thereof. The method takes the benzylamine or benzylamine derivative and Bununte salt as a raw material, takes N, N - dimethylformamide as a solvent, fully reacts under 70~90 °C, and after the reaction is finished, the reaction liquid is separated and purified to obtain N - thienylbenzimide or a derivative thereof. The method is simple and safe, no oxidizing agent and additives exist, cuprous bromide is added as a catalyst, and the reaction temperature is lowered, and the reaction temperature is lowered. The method improves the yield, avoids the use of raw materials such as mercaptan and the like, is less in three wastes, and is environment-friendly. (by machine translation)

A New Synthetic Method for Sulphenimines. Fluoride-catalysed Reaction of N,N-Bis(trimethylsilyl)sulphenamides with Aldehydes and Ketones

Morimoto, Toshiaki,Nezu, Yoshitaka,Achiwa, Kazuo,Sekiya, Minoru

, p. 1584 - 1585 (2007/10/02)

A convenient, general method for the preparation of sulphenimines by the reaction of aldehydes and ketones with N,N-bis(trimethylsilyl)sulphenamides in the presence of tetrabutylammonium fluoride catalyst is described.

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