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832090-73-0

832090-73-0

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  • 3-[NITROSO(PHENYLMETHOXY)AMINO]-N-[(PHENYLMETHOXY)CARBONYL]-L-ALANINE; 3-[NITROSO(BENZYLOXY)AMINO]-N-(CARBOBENZYLOXY)-L-ALANINE

    Cas No: 832090-73-0

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832090-73-0 Usage

Chemical Properties

Pale Yellow Solid

Uses

Intermediate for synthesis of L-Alanosine.

Check Digit Verification of cas no

The CAS Registry Mumber 832090-73-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,2,0,9 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 832090-73:
(8*8)+(7*3)+(6*2)+(5*0)+(4*9)+(3*0)+(2*7)+(1*3)=150
150 % 10 = 0
So 832090-73-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H19N3O6/c22-17(23)16(19-18(24)26-12-14-7-3-1-4-8-14)11-21(20-25)27-13-15-9-5-2-6-10-15/h1-10,16H,11-13H2,(H,19,24)(H,22,23)/t16-/m0/s1

832090-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-3-[nitroso(phenylmethyloxy)amino]-N-[(phenylmethyloxy)carbonyl]alanine

1.2 Other means of identification

Product number -
Other names 3-[Nitroso(benzyloxy)amino]-N-[(benzyloxy)carbonyl]-L-alanine

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:832090-73-0 SDS

832090-73-0Downstream Products

832090-73-0Relevant articles and documents

An improved stereoselective synthesis of L-alanosine

Strazzolini, Paolo,Dall'Arche, Maria Grazia,Zossi, Maura,Pavsler, Andrea

, p. 4710 - 4716 (2007/10/03)

An improved, stereoselective synthesis of the natural, non-proteogenic amino acid L-alanosine has been developed, starting from the readily available and cheap substrate L-serine, in six steps and 49% overall yield. The process is very efficient, is suitable for large-scale production, and affords L-alanosine with properties comparable with those of the natural substance. In addition, the structural assignment concerning some previously reported synthetic alkylated derivatives of the natural amino acid has been definitively confirmed. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

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