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Carbamic acid, [(3S)-1-(diaminophosphinyl)hexahydro-2-oxo-1H-azepin-3-yl]-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

307345-56-8

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307345-56-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 307345-56-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,7,3,4 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 307345-56:
(8*3)+(7*0)+(6*7)+(5*3)+(4*4)+(3*5)+(2*5)+(1*6)=128
128 % 10 = 8
So 307345-56-8 is a valid CAS Registry Number.

307345-56-8SDS

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 (3S)-3-benzyloxycarbonylamino-1-diaminophosphoryl-2-perhydroazepinone

1.2 Other means of identification

Product number -
Other names 3(S)-benzyloxycarbonylamino-1-diaminophosphinyl-2-caprolactam

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:307345-56-8 SDS

307345-56-8Downstream Products

307345-56-8Relevant academic research and scientific papers

Synthesis and biological activity of sulphostin analogues, novel dipeptidyl peptidase IV inhibitors

Abe, Masatoshi,Akiyama, Tetsuo,Umezawa, Yoji,Yamamoto, Keiichiro,Nagai, Masashi,Yamazaki, Hiroko,Ichikawa, Yuh-Ichiro,Muraoka, Yasuhiko

, p. 785 - 797 (2007/10/03)

The structure of sulphostin (1), a novel dipeptidyl peptidase IV (DPP-IV) inhibitor, is consisted of three key functional groups, including a characteristic amino(sulfoamino)phosphinyl group, on a piperidine ring. To examine the relationship between its s

SULPHOSTIN ANALOGUES AND PROCESSES FOR THE PREPARATION OF SULPHOSTIN AND ANALOGUES THEREOF

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Example 8, (2008/06/13)

A sulphostin analogue represented by the general formula, wherein n is an integer of from 0 to 3, provided that a case where n is 2 and steric configurations of C* and P* are S and R, respeetively, is excluded, or a pharmaceutically acceptable salt thereof.

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