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Tert-Butyl (R)-a-AMino-cyclohexanepropanoate is a versatile chemical compound characterized by the presence of a tert-butyl group, an (R)-a-amino-cyclohexane ring, and a propanoate functional group. tert-Butyl (R)-a-AMino-cyclohexanepropanoate is recognized for its steric hindrance provided by the tert-butyl group, the stereochemistry introduced by the (R)-a-amino-cyclohexane ring, and the propanoate group's capacity for facile manipulation and molecular attachment. It plays a significant role in organic chemistry and drug development, offering a valuable chiral building block for the synthesis of pharmaceuticals and other organic compounds.

193286-94-1

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193286-94-1 Usage

Uses

Used in Pharmaceutical Synthesis:
Tert-Butyl (R)-a-AMino-cyclohexanepropanoate is utilized as a chiral building block for the creation of pharmaceuticals, leveraging its unique structural features to contribute to the development of complex molecules with specific biological activities.
Used in Organic Chemistry Research:
In the realm of organic chemistry, Tert-Butyl (R)-a-AMino-cyclohexanepropanoate serves as a key intermediate in the synthesis of various organic compounds, taking advantage of its sterically hindered and stereochemically rich structure to facilitate innovative chemical reactions and molecule constructions.
Used in Drug Development:
Tert-Butyl (R)-a-AMino-cyclohexanepropanoate is employed as a crucial component in drug development, where its versatility allows for the design and synthesis of new pharmaceutical agents with potential therapeutic applications, enhancing the repertoire of available treatments for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 193286-94-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,2,8 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 193286-94:
(8*1)+(7*9)+(6*3)+(5*2)+(4*8)+(3*6)+(2*9)+(1*4)=171
171 % 10 = 1
So 193286-94-1 is a valid CAS Registry Number.

193286-94-1SDS

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)-TERT-BUTYL 2-AMINO-3-CYCLOHEXYLPROPANOATE

1.2 Other means of identification

Product number -
Other names (R)-TERT-BUTYL 2-AMINO-3-CYCLOHEXYLPROPANOATE

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:193286-94-1 SDS

193286-94-1Relevant academic research and scientific papers

An efficient asymmetric biomimetic transamination of α-keto esters to chiral α-amino esters

Xiao, Xiao,Liu, Mao,Rong, Chao,Xue, Fazhen,Li, Songlei,Xie, Ying,Shi, Yian

supporting information, p. 5270 - 5273 (2013/01/15)

An efficient asymmetric biomimetic transamination of α-keto esters with quinine derivatives as chiral bases was described. A wide variety of α-amino esters containing various functional groups can be synthesized in high yield and enantioselectivity.

An efficient preparation of the potent and selective pseudopeptide thrombin inhibitor, inogatran

Preville, Patrice,He, John X.,Tarazi, Micheline,Siddiqui, M. Arshad,Cody, Wayne L.,Doherty, Annette M.

, p. 1563 - 1566 (2007/10/03)

Inogatran is an effective and selective pseudopeptide inhibitor of thrombin that has been shown to be efficacious in a series of in vitro and in vivo models of thrombosis. Herein, we report an efficient and convergent chemical synthesis of Inogatran that is amenable to the preparation of multiple gram quantities.

A nonpeptidic agonist ligand of the human C5a receptor: Synthesis, binding affinity optimization and functional characterization

De Laszlo,Allen,Li,Ondeyka,Rivero,Malkowitz,Molineaux,Siciliano,Springer,Greenlee,Mantlo

, p. 213 - 218 (2007/10/03)

The structural optimization for binding affinity and attempted modification of agonist function of a nonpeptide ligand of the human C5a receptor is described.

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