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N-propylglycine, also known as 1-aminopropane-1-carboxylic acid, is an organic compound with the chemical formula C5H11NO2. It is a derivative of glycine, an amino acid, with a propyl group (a three-carbon alkyl chain) attached to the nitrogen atom. N-propylglycine is a zwitterion, meaning it has both a positive and a negative charge at different sites within the molecule. N-propylglycine is a white crystalline solid that is soluble in water and has a role as a building block in the synthesis of various pharmaceuticals and other chemical compounds. It is also used in the preparation of surfactants and as a chiral auxiliary in asymmetric synthesis.

6939-13-5

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6939-13-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6939-13-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6939-13:
(6*6)+(5*9)+(4*3)+(3*9)+(2*1)+(1*3)=125
125 % 10 = 5
So 6939-13-5 is a valid CAS Registry Number.

6939-13-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(propylamino)acetic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names N-propylglycine hydrochloride

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:6939-13-5 SDS

6939-13-5Relevant academic research and scientific papers

Synthesis, characterization, spectroscopy, cytotoxic activity and molecular dynamic study on the interaction of three palladium complexes of phenanthroline and glycine derivatives with calf thymus DNA

Ajloo, Davood,Eslami Moghadam, Mahboube,Ghadimi, Khadijeh,Ghadamgahi, Maryam,Saboury, Ali Akbar,Divsalar, Adeleh,Sheikhmohammadi, Minoo,Yousefi, Khalil

, p. 144 - 160 (2015/03/31)

The interaction of three novel synthesized complexes of [Pd(phen)(R-gly)]NO3, where R-gly is methyl-, propyl-, and amyl-glycine; and phen is 1,10-phenanthroline were synthesized and characterized by spectroscopic methods. The interaction of ct-

PRO-DRUG COMPOUNDS

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Page/Page column 23-24, (2014/01/18)

A compound of formula (I), or a pharmaceutically acceptable salt thereof: wherein Z1, Z2, and Z3, Q, R2, A, and R1 are as defined in the claims.

Pro-drug Compounds

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Paragraph 0176; 0177, (2014/02/15)

A compound of formula (I), or a pharmaceutically acceptable salt thereof: The compound is used in pharmaceutical compositions and in a method of treatment of a disease or medical condition which benefits from inhibition of gap junction activity by administering to a subject suffering from such disease or condition.

Polypeptoids from n-substituted glycine n-carboxyanhydrides: Hydrophilic, hydrophobic, and amphiphilic polymers with poisson distribution

Fetsch, Corinna,Grossmann, Arlett,Holz, Lisa,Nawroth, Jonas F.,Luxenhofer, Robert

experimental part, p. 6746 - 6758 (2012/03/10)

Preparation of defined and functional polymers has been one of the hottest topics in polymer science and drug delivery in the recent decade. Also, research on (bio)degradable polymers gains more and more interest, in particular at the interface of these t

Synthesis of Strombine. A New Method for Monocarboxymethylation of Primary Amines

Kihlberg, Jan,Bergman, Rolf,Wickberg, Boerje

, p. 911 - 916 (2007/10/02)

Many common methods for monocarboxymethylation of primary amines give various amounts of dialkylated by-products.In this work the reaction of two equivalents of glyoxilic acid with representative primary aliphatic and aromatic amines, as well as with amino acids and a dipeptide, is shown to give only the N-(carboxymethyl)-N-formyl derivative of the amine under mild conditions in carboxylic acid solvents.Hydrolysis then produces the monocarboxymethylated primary amine in good to exellent overall yield.Proof that the intermediate product is not obtained via the Leuckart reaction is given.

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