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1,2-Pyrrolidinedicarboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-, 2-methyl 1-(phenylmethyl) ester, (2R,4R)is a chiral chemical compound with the molecular formula C19H27NO5. It is a derivative of 1,2-pyrrolidinedicarboxylic acid and is commonly used in the field of organic chemistry as a chiral building block for the synthesis of pharmaceuticals and biologically active compounds. 1,2-Pyrrolidinedicarboxylic acid,
4-[[(1,1-dimethylethoxy)carbonyl]amino]-, 2-methyl 1-(phenylmethyl)
ester, (2R,4R)has potential applications in drug development and research due to its unique structural and stereochemical properties. Additionally, it may also find utility as an intermediate in the production of other chemicals and materials.

787615-48-9

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787615-48-9 Usage

Uses

Used in Pharmaceutical Industry:
1,2-Pyrrolidinedicarboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-, 2-methyl 1-(phenylmethyl) ester, (2R,4R)is used as a chiral building block for the synthesis of pharmaceuticals and biologically active compounds. Its unique structural and stereochemical properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Research and Development:
1,2-Pyrrolidinedicarboxylic acid,
4-[[(1,1-dimethylethoxy)carbonyl]amino]-, 2-methyl 1-(phenylmethyl)
ester, (2R,4R)is used in research and development for the exploration of its potential applications in drug development. Its unique properties and chiral nature make it an interesting subject for scientific studies and the development of novel pharmaceuticals and biologically active compounds.
Used as an Intermediate in Chemical Production:
1,2-Pyrrolidinedicarboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-, 2-methyl 1-(phenylmethyl) ester, (2R,4R)may also find utility as an intermediate in the production of other chemicals and materials. Its unique structure and properties can be leveraged to create new compounds and materials with various applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 787615-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,7,6,1 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 787615-48:
(8*7)+(7*8)+(6*7)+(5*6)+(4*1)+(3*5)+(2*4)+(1*8)=219
219 % 10 = 9
So 787615-48-9 is a valid CAS Registry Number.

787615-48-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,4R)-N-1-(benzyloxycarbonyl)-4-(tert-butyloxycarbonylamino)proline methyl ester

1.2 Other means of identification

Product number -
Other names tert-butyl (3R,5R)-1-((benzyloxy)carbonyl)-5-(methoxycarbonyl)pyrrolidin-3-ylcarbamate

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:787615-48-9 SDS

787615-48-9Relevant academic research and scientific papers

Chimeric (aeg-pyrrolidine)PNAs: Synthesis and stereo-discriminative duplex binding with DNA/RNA

Lonkar, Pallavi S.,Ganesh, Krishna N.,Kumar, Vaijayanti A.

, p. 2604 - 2611 (2007/10/03)

The design and facile conversion of naturally occurring 4-hydroxyproline to all four diastereomers of thymine pyrrolidine PNA monomer, (2R,4S)-adenine, -guanine and -cytosine monomers and their incorporation into duplex forming PNA oligomers is reported,

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