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35010-96-9

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35010-96-9 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 35010-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,1 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35010-96:
(7*3)+(6*5)+(5*0)+(4*1)+(3*0)+(2*9)+(1*6)=79
79 % 10 = 9
So 35010-96-9 is a valid CAS Registry Number.

35010-96-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl (2S)-2-[(2-amino-2-oxoethyl)carbamoyl]pyrrolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names N-benzyloxycarbonyl-L-prolylglycinamide

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:35010-96-9 SDS

35010-96-9Relevant articles and documents

PEPTIDE DEFORMYLASE INHIBITORS

-

Page/Page column 24-25, (2010/11/27)

Novel PDF inhibitors of Formula (I), pharmaceutical compositions thereof and their use in treating bacterial infections are described.

Large-Scale Synthesis of Mammalian Gonadoliberin without Protection of Side-Chain Functions

Masiukiewicz, Elzbieta,Rzeszotarska, Barbara

, p. 41 - 47 (2007/10/02)

A simple, large-scale preparation of mammalian gonadoliberin was elaborated using classical solution methods without protecting side-chain functions.At the final stage, a hexapeptide segment was condensed with the corresponding tetrapeptide and the obtain

SYNTHESIS OF 3(NH2); Pro3; D-Ala6>- and 2(NO2); Pro3; D-Ala6>LULIBERINS

Burov, S. V.,Kaurov, O. A.,Martynov, V. F.,Smirnova, M. P.

, p. 518 - 524 (2007/10/02)

In order to study the influence of substituents of the aromatic ring of D-phenylalanine on the inhibiting capacity of luliberian analogs, we have synthesized two new analogs: 2; Pro3; D-Ala6>- and

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