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16305-78-5

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16305-78-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16305-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,0 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16305-78:
(7*1)+(6*6)+(5*3)+(4*0)+(3*5)+(2*7)+(1*8)=95
95 % 10 = 5
So 16305-78-5 is a valid CAS Registry Number.

16305-78-5SDS

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 benzyl 2-[2-(phenylmethoxycarbonylamino)propanoylamino]acetate

1.2 Other means of identification

Product number -
Other names N-Benzyloxycarbonyl-L-alanyl-glycin-benzylester

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:16305-78-5 SDS

16305-78-5Relevant articles and documents

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Stelakatos,G.C.

, p. 4222 - 4224 (1961)

-

1-(o-NITROPHENYLSULPHONYLOXY)BENZOTRIAZOLE, REAGENT FOR THE CONDENSATION OF CARBOXYLIC ACIDS WITH AMINES

Topuzyan, V. O.,Martirosyan, M. S.

, p. 2148 - 2153 (2007/10/02)

With the Schotten-Baumann reaction we have synthesized 1-(o-nitrophenylsulfonyloxy)benzotriazole and have shown its suitability for the synthesis of esters of 1-hydroxybenzotriazole and carboxylic amides, and also of peptides.

STUDIES ON AMINO ACIDS AND PEPTIDES-I SYNTHESIS OF N-BENZYLOXYCARBONYLENDOTHIODIPEPTIDE ESTERS

Clausen, K.,Thorsen, M.,Lawesson, S.-O.

, p. 3635 - 3639 (2007/10/02)

N-Benzyloxycarbonylendothiodipeptide esters, 3, are synthesized without racemization from the corresponding N-benzyloxycarbonyldipeptide esters, 2, using 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane 2,4-disulfide, 1, as thionation reagent.The benzyloxycarbonyl amino-protecting group (Z) is removed from 3 by using HBr-AcOH.

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