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13318-97-3

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13318-97-3 Usage

Occurrence

Naturally occurring in certain marine organisms, including some species of sponges and bacteria

Classification

Acidic amino acid derivative

Research Interest

Studied for potential pharmaceutical and medicinal properties

Potential Applications

Investigated as a potential treatment for cancer and other diseases

Structure

Unique molecular structure drives further research into its properties and potential uses

Check Digit Verification of cas no

The CAS Registry Mumber 13318-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,1 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13318-97:
(7*1)+(6*3)+(5*3)+(4*1)+(3*8)+(2*9)+(1*7)=93
93 % 10 = 3
So 13318-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H12N2O2/c1-3(7-2)4(6)5(8)9/h3-4,7H,6H2,1-2H3,(H,8,9)

13318-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-3-N-methylaminobutyric acid

1.2 Other means of identification

Product number -
Other names Benzenamine,3,6-dimethyl-2-nitro

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:13318-97-3 SDS

13318-97-3Upstream product

13318-97-3Downstream Products

13318-97-3Relevant articles and documents

Stereochemical elucidation and total synthesis of dihydropacidamycin D, a semisynthetic pacidamycin

Boojamra,Lemoine,Lee,Leger,Stein,Vernier,Magon,Lomovskaya,Martin,Chamberland,Lee,Hecker,Lee

, p. 870 - 874 (2007/10/03)

Hydrogenation of the C(4′) exocyclic olefin of the pacidamycins has been shown to produce a series of semisynthetic compounds, the dihydropacidamycins, with antimicrobial activity similar to that of the natural products. Elucidation of stereochemistry in

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