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Phosphonic acid, (2-amino-4-phenylbutyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82102-19-0

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82102-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82102-19-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,0 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82102-19:
(7*8)+(6*2)+(5*1)+(4*0)+(3*2)+(2*1)+(1*9)=90
90 % 10 = 0
So 82102-19-0 is a valid CAS Registry Number.

82102-19-0SDS

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 (2-amino-4-phenylbutyl)phosphonic acid

1.2 Other means of identification

Product number -
Other names Phosphonic acid,(2-amino-4-phenylbutyl)

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:82102-19-0 SDS

82102-19-0Downstream Products

82102-19-0Relevant academic research and scientific papers

Preparation of 1-aminoalkylphosphonic acids and 2-aminoalkylphosphonic acids by reductive amination of oxoalkylphosphonates

Ryglowski, Artur,Kafarski, Pawel

, p. 10685 - 10692 (2007/10/03)

By reacting dialkyl 1-oxo- or 2-oxoalkylphosphonates with benzhydrylamine followed by reduction with triacetoxyborohydride and acid hydrolysis gave corresponding aminoalkylphosphonic acids with satisfactory yields. The use of benzylamine, α-methylbenzylamine and tritylamine was unsuccessful in the case of dialkyl 1-oxoalkylphosphonates whereas conversion of 2-oxoalkylphosphonates was also achieved although with lower yields.

PREPARATION OF OPTICALLY ACTIVE 2-AMINOALKYLPHOSPHINIC AND PHOSPHONIC ACIDS

Duggan, Mark E.,Karanewsky, Donald S.

, p. 2935 - 2938 (2007/10/02)

The reaction of sodium alkylphosphinates or sodium dialkylphosphonates with tosylamino tosylates of amino alcohols derived from 1-aminoalkylcarboxylic acids gives high yields of optically active 2-tosylaminoalkylphosphinic or phosphonic esters.

ANIMATION REDUCTRICE DES β-CETOPHOSPHONATES: PREPARATION D'ACIDES AMINOALKYLPHOSPHONIQUES

Varlet, J. M.,Collignon, N.,Savignac, Ph.

, p. 3713 - 3721 (2007/10/02)

Diethyl 2-oxo-alkylphosphonates undergo reductive amination in the presence of an amine and sodium cyanohydridoborate (NaBH3CN) in MeOH at Ph 7-7.5.Studies with a large variety of ketophosphonates show that the reaction rate is very sensitive to steric hi

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