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3-(1-PHENYLETHYLAMINO)PROPANOIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95350-05-3

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95350-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95350-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,5 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95350-05:
(7*9)+(6*5)+(5*3)+(4*5)+(3*0)+(2*0)+(1*5)=133
133 % 10 = 3
So 95350-05-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO2/c1-9(12-8-7-11(13)14)10-5-3-2-4-6-10/h2-6,9,12H,7-8H2,1H3,(H,13,14)

95350-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1-PHENYLETHYLAMINO)PROPANOIC ACID

1.2 Other means of identification

Product number -
Other names 3-[(1-phenylethyl)amino]propanoic acid

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:95350-05-3 SDS

95350-05-3Relevant academic research and scientific papers

Synthesis and Stereochemistry of Chiral Azetidin-2-ones and Azetidine-2-thiones. I. Synthesis of Diastereomeric 2- and 3-Substituted N-(α-Methylbenzyl)-β-aminopropionic Acids

Romanova, N. N.,Tallo, T. G.,Bundel', Yu. G.

, p. 375 - 377 (2007/10/03)

Nucleophilic addition of α-methylbenzylamine to the double bond of 2- and 3-substituted acrylic acids in pyridine under reflux proceeds nonstereoselectively.

SYNTHESIS OF 1-(α-PHENYLETHYL)AZETIDIN-2-ONES

Romanova, N. N.,Budylin, V. A.,Grishina, G. V.,Potapov, V. M.,Torocheshnikov, V. N.,et al.

, p. 1354 - 1357 (2007/10/02)

Phase-transfer catalyzed cyclization of racemic and optically active N-substituted β-aminoacids has given racemic and optically active 2-azetidinones, the spatial structures of which have been established by NMR spectroscopy.The original β-aminoacids were

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