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80999-51-5

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80999-51-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80999-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,9 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80999-51:
(7*8)+(6*0)+(5*9)+(4*9)+(3*9)+(2*5)+(1*1)=175
175 % 10 = 5
So 80999-51-5 is a valid CAS Registry Number.

80999-51-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S)-2,3-diaminobutanoic acid

1.2 Other means of identification

Product number -
Other names α,β-Diaminobuttersaeure

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:80999-51-5 SDS

80999-51-5Downstream Products

80999-51-5Relevant articles and documents

Totopotensamides, polyketide-cyclic peptide hybrids from a mollusk-associated bacterium Streptomyces sp.

Lin, Zhenjian,Flores, Malem,Forteza, Imelda,Henriksen, Niel M.,Concepcion, Gisela P.,Rosenberg, Gary,Haygood, Margo G.,Olivera, Baldomero M.,Light, Alan R.,Cheatham, Thomas E.,Schmidt, Eric W.

experimental part, p. 644 - 649 (2012/06/29)

Two new compounds, the peptide-polyketide glycoside totopotensamide A (1) and its aglycone totopotensamide B (2), were isolated from a Streptomyces sp. cultivated from the gastropod mollusk Lienardia totopotens collected in the Philippines. The compounds contain a previously undescribed polyketide component, a novel 2,3-diaminobutyric acid-containing macrolactam, and a new amino acid, 4-chloro-5,7-dihydroxy-6-methylphenylglycine. The application of Marfey's method to phenylglycine derivatives was explored using quantum mechanical calculations and NMR.

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