(R)-1-PHOSPHONO-BENZYLAMINE

Base Information

Chemical Name:(R)-1-PHOSPHONO-BENZYLAMINE
CAS No.:37714-05-9
Molecular Formula:C7H10 N O3 P
Molecular Weight:187.135
Hs Code.:2931900090
Mol file:37714-05-9.mol

Synonyms:Phosphonicacid, (aminophenylmethyl)-, (R)-; Phosphonic acid, [(R)-aminophenylmethyl]-(9CI); ((R)-a-Aminobenzyl)phosphonicacid; (+)-a-Aminobenzylphosphonic acid;(R)-(Amino(phenyl)methyl)phosphonic acid; (R)-Phosphophenylglycine

Suppliers and Price of (R)-1-PHOSPHONO-BENZYLAMINE

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
(R)-1-AMINO-BENZYLPHOSPHONIC ACID 95.00%
5MG
$ 497.89

Total 4 raw suppliers

Chemical Property of (R)-1-PHOSPHONO-BENZYLAMINE

Chemical Property:

PSA：93.36000
LogP:1.52190

Purity/Quality:

98% ^*data from raw suppliers

(R)-1-AMINO-BENZYLPHOSPHONIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

General Description (R)-1-Phosphono-benzylamine, also known by various synonyms such as (R)-(Amino(phenyl)methyl)phosphonic acid or (R)-Phosphophenylglycine, is an optically pure α-aminophosphonic acid. It can be synthesized through a convenient route involving the reaction of hypophosphorous acid salts of (R)-(+)-N-α-methylbenzylamine with aldehydes, followed by simultaneous deprotection and oxidation to yield the product in high optical purity. Additionally, chiral α-aminophosphonic acids like (R)-1-PHOSPHONO-BENZYLAMINE can be prepared via diastereoselective addition of phosphite or phosphonate anions to enantiopure sulfinimines, demonstrating its accessibility through asymmetric synthetic methods.

Technology Process of (R)-1-PHOSPHONO-BENZYLAMINE

There total 50 articles about (R)-1-PHOSPHONO-BENZYLAMINE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.0%

: 1201762-38-0
C₁₈H₂₂NO₄P

: 37714-05-9
(R)-1-amino-1-phenylmethylphosphonic acid

Guidance literature:: C₁₈H₂₂NO₄P; With hydrogenchloride; water; for 16h; Inert atmosphere; Reflux;

With methyloxirane; In ethanol; at 20 ℃; for 3h; Inert atmosphere;
DOI:10.1002/chem.200901901