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98266-32-1

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98266-32-1 Usage

Chemical Properties

White powder

Uses

(αR)?-α-?[[(1,?1-Dimethylethoxy)?carbonyl]?amino]?-?2-pyridinepropanoic Acid is an intermediate used to prepare heterocyclic amides as nitric oxide production inhibitors.

Check Digit Verification of cas no

The CAS Registry Mumber 98266-32-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,2,6 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98266-32:
(7*9)+(6*8)+(5*2)+(4*6)+(3*6)+(2*3)+(1*2)=171
171 % 10 = 1
So 98266-32-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H18N2O4/c1-13(2,3)19-12(18)15-10(11(16)17)8-9-6-4-5-7-14-9/h4-7,10H,8H2,1-3H3,(H,15,18)(H,16,17)/p-1/t10-/m1/s1

98266-32-1SDS

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 (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-pyridin-2-ylpropanoic acid

1.2 Other means of identification

Product number -
Other names Boc-3-(2-pyridyl)-D-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:98266-32-1 SDS

98266-32-1Relevant articles and documents

BICYCLIC COMPOUNDS

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Paragraph 00375, (2020/10/28)

Provided herein are compounds and pharmaceutical compositions comprising said compounds that are useful for treating cancers. Specific cancers include those that are mediated by YAP/TAZ or those that are modulated by the interaction between YAP/TAZ and TEAD.

Studies on polypeptides XXXII. Solid-phase synthesis of RNase S-peptide 1-14 analogues; replacement of histidine-12 by β-(2-pyridyl)-L-alanine and β-(4-pyridyl)-L-alanine

Hoes, C.,Raap, J.,Bloemhoff, W.,Kerling, K. E. T.

, p. 99 - 104 (2007/10/02)

The synthesis of two analogues of the N-terminal tetradecapeptide of ribonuclease A (RNase S-peptide 1-14), in which the active site histidine-12 residue is replaced by β-(2-pyridyl)-L-alanine and β-(4-pyridyl)-L-alanine, has been accomplished by the solid-phase method.The enantiomers of β-(2-pyridyl)alanine were obtained by chymotryptic hydrolysis of its racemic Nα-acetyl ethyl ester.The Boc derivative of both L-amino acids has been synthesized.

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