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(R)-1-CBZ-2-CYANO-PYRROLIDINE is a chiral pyrrolidine derivative characterized by its (R)-configuration and a carbobenzyloxy (CBZ) functional group attached to the nitrogen atom. The incorporation of a cyano group at the 2-position of the pyrrolidine ring endows it with versatility for use in the synthesis of pharmaceuticals and agrochemicals. As a key intermediate, it is highly valued in the pharmaceutical industry for its unique structural properties and reactivity, serving as a building block in the creation of complex organic molecules with therapeutic applications.

620601-77-6

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620601-77-6 Usage

Uses

Used in Pharmaceutical Industry:
(R)-1-CBZ-2-CYANO-PYRROLIDINE is used as a key intermediate for the synthesis of various pharmaceuticals due to its unique structural properties and reactivity. It plays a crucial role in the development of drugs with therapeutic applications, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
(R)-1-CBZ-2-CYANO-PYRROLIDINE is also utilized as an intermediate in the synthesis of agrochemicals, where its versatility and reactivity are harnessed to create compounds with potential applications in agriculture, such as pesticides or plant growth regulators.
Used in Chemical Research and Development:
In the realm of chemical research and development, (R)-1-CBZ-2-CYANO-PYRROLIDINE serves as a valuable compound for exploring new synthetic pathways and developing innovative methodologies. Its unique characteristics make it an essential tool for scientists working on the frontiers of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 620601-77-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,0,6,0 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 620601-77:
(8*6)+(7*2)+(6*0)+(5*6)+(4*0)+(3*1)+(2*7)+(1*7)=116
116 % 10 = 6
So 620601-77-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H14N2O2/c14-9-12-7-4-8-15(12)13(16)17-10-11-5-2-1-3-6-11/h1-3,5-6,12H,4,7-8,10H2/t12-/m1/s1

620601-77-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-1-Cbz-2-Cyano-Pyrrolidine

1.2 Other means of identification

Product number -
Other names benzyl (2R)-2-cyanopyrrolidine-1-carboxylate

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:620601-77-6 SDS

620601-77-6Relevant articles and documents

Total Synthesis of the Marine Natural Product Hemiasterlin by Organocatalyzed α-Hydrazination

Lang, Jan Hendrik,Jones, Peter G.,Lindel, Thomas

, p. 12714 - 12717 (2017/09/25)

An efficient synthesis of the potently cytotoxic marine peptide hemiasterlin is presented. The tetramethyltryptophan moiety is assembled by tert-prenylation of indole, followed by the high-yielding organocatalyzed α-hydrazination of a sterically congested aldehyde with excellent enantioselectivity. 2-Bromo-N-ethylpyridinium tetrafluoroborate (BEP)-mediated peptide coupling completes the synthesis, being the first approach that does not employ chiral auxiliaries. A novel phenonium-type rearrangement of the indole system occurred when subjecting dihydroxylated 3-tert-prenylindole to Mitsunobu conditions.

Novel pyrrolidine heterocycles as CCR1 antagonists

Merritt, J. Robert,James, Ray,Paradkar, Vidyadhar M.,Zhang, Chongwu,Liu, Ruiyan,Liu, Jinqi,Jacob, Biji,Chiriac, Camelia,Ohlmeyer, Michael J.,Quadros, Elizabeth,Wines, Pamela,Postelnek, Jennifer,Hicks, Catherine M.,Chen, Weiqing,Kimble, Earl F.,O'Brien, Linda,White, Nicole,Desai, Hema,Appell, Kenneth C.,Webb, Maria L.

supporting information; experimental part, p. 5477 - 5479 (2010/12/24)

A novel series of pyrrolidine heterocycles was prepared and found to show potent inhibitory activity of CCR1 binding and CCL3 mediated chemotaxis of a CCR1-expressing cell line. A potent, optimized triazole lead from this series was found to have acceptab

ORTHO PYRROLIDINE, BENZYL-SUBSTITUTED HETEROCYCLE CCR1 ANTAGONISTS FOR AUTOIMMUNE DISEASES and INFLAMMATION

-

Page/Page column 29-30, (2009/04/24)

Compounds of the formula are disclosed. The compounds are CCR1 antagonists which are useful for the treatment and prevention of inflammatory and autoimmune diseases. Other embodiments are also disclosed.

Organocatalysis with proline derivatives: Improved catalysts for the asymmetric Mannich, nitro-Michael and aldol reactions

Cobb, Alexander J. A.,Shaw, David M.,Longbottom, Deborah A.,Gold, Johan B.,Ley, Steven V.

, p. 84 - 96 (2007/10/03)

Tetrazole and acylsulfonamide organocatalysts derived from proline have been synthesised and applied to the asymmetric Mannich, nitro-Michael and aldol reactions to give results that are superior to the proline-catalysed counterpart.

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