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L-Proline, N-[(phenylmethoxy)carbonyl]-D-2-aminobutanoyl- is a complex organic compound with the chemical formula C16H20N2O4. It is a derivative of L-proline, an essential amino acid, and features a phenylmethoxycarbonyl group attached to the nitrogen atom. L-Proline, N-[(phenylmethoxy)carbonyl]-D-2-aminobutanoyl- is characterized by its unique structure, which includes a cyclic secondary amine and a chiral center, making it a valuable building block in the synthesis of various pharmaceuticals and biologically active molecules. Its specific structure allows for the formation of peptide bonds and other important chemical reactions, contributing to its significance in the field of organic chemistry and drug development.

2900-22-3

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2900-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2900-22-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,0 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2900-22:
(6*2)+(5*9)+(4*0)+(3*0)+(2*2)+(1*2)=63
63 % 10 = 3
So 2900-22-3 is a valid CAS Registry Number.

2900-22-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Z-D-Abu-Pro

1.2 Other means of identification

Product number -
Other names Benzyloxycarbonyl-D-α-amino-butyryl-L-prolin

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:2900-22-3 SDS

2900-22-3Relevant academic research and scientific papers

THE SYNTHESIS OF A Nγ-PHTHALYL-Nα-METHYL-α,γ-DIAMINOBUTYRYL CONGENER OF VIRGINIAMYCIN S1

Anteunis, M. J. O.,Auwera, C. Van der,Vanfleteren, L.,Borremans, F.

, p. 135 - 148 (2007/10/02)

A synthesis of (A2bu=α,γ-diaminobutyric acid) is reported using the very efficient coupling agent BOP-Cl (N,N'-bis(3-oxo-2-oxazolidinyl)phosphinic chloride) for imino acid peptide bond formation.The total yield is 11percent for the 5 coupling steps and one lactonization.The final step was a cyclization between residues 5 and 6, after (I) first t-Boc acidic deprotection with 85percent HCOOH of the linear precursor Z-Thr(Nα-Boc-Phg-O-)-D-Abu-Pro-MePhe-MeA2bu(γPht)-OBut followed by (ii) acidic saponification (Tfa) of the t-Bu ester.This sequence was found to be prerequisite, in view of the extreme lability of the 4-5 peptide bond under acidic conditions.

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