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L-AZATYROSINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58525-82-9

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58525-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58525-82-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,2 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58525-82:
(7*5)+(6*8)+(5*5)+(4*2)+(3*5)+(2*8)+(1*2)=149
149 % 10 = 9
So 58525-82-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O3/c9-8(10(12)13)5-6-1-3-7(11)4-2-6/h1-4,8,11H,5,9H2/t8-/m1/s1

58525-82-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name L-AZATYROSINE

1.2 Other means of identification

Product number -
Other names 4-Nitro-3-phenyl-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:58525-82-9 SDS

58525-82-9Relevant academic research and scientific papers

Efficient large-scale synthesis of Boc-L-azatyrosine

Germain, Herve,Harris, Craig S.,Renaud, Fabrice,Warin, Nicolas

experimental part, p. 523 - 530 (2009/06/20)

A rapid and convenient process for the synthesis of Boc-L-azatyrosine is described from commercially available Boc-β-iodo-Ala-OMe. Copyright Taylor & Francis Group, LLC.

A stereocontrolled synthesis of (R)- and (S)-azatyrosine

Cremonesi, Giuseppe,Dalla Croce, Piero,La Rosa, Concetta,Pizzatti, Enrica

, p. 563 - 567 (2007/10/03)

An asymmetric synthesis of (R)- or (S)- azatyrosine, starting from (2S)- or (2R)-2,5-dihydro-3,6-dimethoxy-2-isopropylpyrazine (5) (Scho?llkopf reagent) and 5-benzenesulfonyloxy-2-hydroxymethylpyridine (3), is reported. The diastereocontrolled addition gi

Enantioselective synthesis of (2-pyridyl)alanines via catalytic hydrogenation and application to the synthesis of L-azatyrosine.

Adamczyk,Akireddy,Reddy

, p. 3157 - 3159 (2007/10/03)

[reaction: see text] A novel method for the synthesis of (2-pyridyl)alanines 2a-b was developed by converting (2-pyridyl)dehydroamino acid derivatives 1a-b to the corresponding N-oxides 3a-b followed by asymmetric hydrogenation using (R,R)-[Rh(Et-DUPHOS)(

Enzymatic synthesis of aza-L-tyrosines

Watkins,Phillips, Robert S.

, p. 2099 - 2100 (2007/10/03)

Tyrosine phenol-lyase from Citrobacter freundii synthesizes 2-aza-L-tyrosine and 3-aza-L-tyrosine from 3-hydroxypyridine and 2-hydroxypyridine, respectively, and ammonium pyruvate.

A concise synthesis of either enantiomer of azatyrosine

Cooper, Margaret S.,Seton, Alison W.,Stevens, Malcolm F. G.,Westwell, Andrew D.

, p. 2613 - 2616 (2007/10/03)

A facile route to either enantiomer of azatyrosine is reported, utilising an efficient enzymic resolution of protected azatyrosine ethyl ester by α-chymotrypsin as a key step.

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