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88081-76-9

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88081-76-9 Usage

General Description

(S)-1-PHOSPHONO-3-METHYL-BUTYLAMINE is a chemical compound that belongs to the category of amines and phosphonates. It is a chiral compound with the (S)-stereoisomer being the active form. This chemical is commonly used in pharmaceutical research and drug development, specifically as a precursor for the synthesis of various pharmaceuticals and organic compounds. Due to its unique structure and properties, it has potential applications in the treatment of certain medical conditions and diseases. Additionally, its ability to bind to specific receptors in the body makes it a valuable candidate for drug design and discovery. Overall, (S)-1-PHOSPHONO-3-METHYL-BUTYLAMINE is an important chemical in the field of medicinal chemistry and holds promise for future therapeutic interventions.

Check Digit Verification of cas no

The CAS Registry Mumber 88081-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,8 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88081-76:
(7*8)+(6*8)+(5*0)+(4*8)+(3*1)+(2*7)+(1*6)=159
159 % 10 = 9
So 88081-76-9 is a valid CAS Registry Number.

88081-76-9SDS

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 [(1S)-1-amino-3-methylbutyl]phosphonic acid

1.2 Other means of identification

Product number -
Other names D-Leucine phosphonate

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:88081-76-9 SDS

88081-76-9Downstream Products

88081-76-9Relevant articles and documents

Preparation of optically active 1-aminoalkylphosphonic acids by stereoselective enzymatic hydrolysis of racemic N-acylated 1-aminoalkylphosphonic acids

Solodenko,Kasheva,Kukhar,Kozlova,Mironenko,Svedas,Belozersky

, p. 3989 - 3998 (2007/10/02)

N-Phenylacetylated derivatives of 1-aminoalkylphosphonic acids were synthesized and high enantioselectivity of their hydrolysis by penicillin acylase (EC 3.5.1.11) was demonstrated. Stereoselective enzymatic hydrolysis of racemic 1-(N-phenylacetylamino) alkylphosphonic acids was used for preparation of enantiomeric 1-aminoalkylphosphonic acids. The kinetic regularities of penicillin acylase catalyzed hydrolysis were established and the biocatalytic process was optimized to increase the optical purity and the yield of the optically active product.

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