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N-(2-phenylethyl)sulfuric diamide, also known as 2-phenylethylsulfamide, is an organic compound with the chemical formula C8H11NO2S. It is a derivative of sulfuric acid, where two hydroxyl groups are replaced by 2-phenylethylamine groups. N-(2-phenylethyl)sulfuric diamide is characterized by its aromatic ring structure and amine functionality, which contribute to its unique chemical properties. It is a white crystalline solid and is used in various chemical reactions and as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Due to its reactivity, it is typically handled with care in a controlled laboratory environment.

710-15-6

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710-15-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 710-15-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 710-15:
(5*7)+(4*1)+(3*0)+(2*1)+(1*5)=46
46 % 10 = 6
So 710-15-6 is a valid CAS Registry Number.

710-15-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(sulfamoylamino)ethylbenzene

1.2 Other means of identification

Product number -
Other names N-(Ethylphenyl)sulfamid

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:710-15-6 SDS

710-15-6Relevant academic research and scientific papers

THERAPEUTIC AGENT FOR DIABETES

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Page/Page column 218-219, (2008/06/13)

The present invention provides an agent for the prophylaxis or treatment of diabetes, which is associated with a ferwer side effects such as body weight gain, adipocyte accumulation, cardiac hypertrophy and the like, and which contains a compound represented by the formula: wherein each symbol is as defined in the specification, or a salt thereof or a prodrug thereof.

Intra- and Intermolecular α-Sulfamidoalkylation Reactions

Lee, Chai-Ho,Kohn, Harold

, p. 6098 - 6104 (2007/10/02)

The utility of α-sulfamidoalkylation processes for the generation of sulfamides has been examined.Select aryl-substituted sulfamides were prepared and then treated with acid.Both intra- and intermolecular α-sulfamidoalkylation transformations were observed to proceed in moderate to good yields.The pathways for these reactions are discussed.The generality of these processes has been demonstrated using N,N'-di(aryl-substituted)sulfamides, and the utility of these reactions was examined for the preparation of cyclic sulfamides of novel structure.

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