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1738-86-9

1738-86-9

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1738-86-9 Usage

Chemical Properties

White powder

Uses

Substrate for measuring pancreatic elastase activity.

Check Digit Verification of cas no

The CAS Registry Mumber 1738-86-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,3 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1738-86:
(6*1)+(5*7)+(4*3)+(3*8)+(2*8)+(1*6)=99
99 % 10 = 9
So 1738-86-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H14N2O6/c19-15(24-14-8-6-13(7-9-14)18(21)22)10-17-16(20)23-11-12-4-2-1-3-5-12/h1-9H,10-11H2,(H,17,20)

1738-86-9 Well-known Company Product Price

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  • TCI America

  • (C0333)  N-Carbobenzoxyglycine 4-Nitrophenyl Ester  >98.0%(HPLC)

  • 1738-86-9

  • 1g

  • 405.00CNY

  • Detail

1738-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name <i>N</i>-Carbobenzoxyglycine 4-Nitrophenyl Ester

1.2 Other means of identification

Product number -
Other names CARBOBENZYLOXYGLYCINE 4-NITROPHENYL ESTER

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:1738-86-9 SDS

1738-86-9Relevant articles and documents

-

Yamazaki,N. et al.

, p. 495 - 496 (1974)

-

Yamazaki,Higashi

, p. 170 (1974)

Peptide coupling of unprotected amino acids through in situ p-nitrophenyl ester formation

Gagnon, Paul,Huang, Xicai,Therrien, Eric,Keillor, Jeffrey W.

, p. 7717 - 7719 (2007/10/03)

Several series of dipeptides and tripeptides were prepared via an activation-coupling method involving the in situ formation of a p-nitrophenyl ester of an (N-protected) amino acid, followed by coupling with an unprotected amino acid in partially aqueous solutions. The resulting peptide is easily isolated by precipitation. In general, the yields obtained are good to excellent and racemization is minimal. This method is particularly advantageous with respect to its simplicity and lack of obligatory side chain protection/deprotection steps.

O-ALKYL S-CHLOROFORMYL DITHIOCARBONATES FOR PEPTIDE SYNTHESIS

Khalikov, Sh.Kh.,Alieva, S.V.,Sobirov, M.M.

, p. 809 - 810 (2007/10/02)

-

Use of the 4-methoxy-2,6-dimethylbenzenesulfonyl (Mds) group to synthesize dynorphin [1-13] and related peptides

Wakimasu,Kitada,Fujino

, p. 2592 - 2597 (2007/10/02)

-

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