267230-48-8

Basic information

• Product Name: Cyclohexanecarboxylic acid, 2-[[(phenylmethoxy)carbonyl]amino]-, (1R,2R)-
• CAS NO: 267230-48-8
• Molecular Formula: C15H19NO4
• Molecular Weight: 277.32
• Mol File: 267230-48-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Cyclohexanecarboxylic acid, 2-[[(phenylmethoxy)carbonyl]amino]-, (1R,2R)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanecarboxylic acid, 2-[[(phenylmethoxy)carbonyl]amino]-, (1R,2R)-(267230-48-8)
• EPA Substance Registry System: Cyclohexanecarboxylic acid, 2-[[(phenylmethoxy)carbonyl]amino]-, (1R,2R)-(267230-48-8)

Safety Data

• Hazardous Substances Data: 267230-48-8(Hazardous Substances Data)

Upstream product

• 100-51-6 benzyl alcohol 
• 96894-64-3 (1R,2R)-1,2-cyclohexanedicarboxylic acid monomethyl ester 
• 267230-27-3 methyl (1R,2R)-2-((tert-butoxycarbonyl)amino)cyclohexane-1-carboxylate 
• 267230-26-2 (1S,2R)-2-tert-butoxycarbonylamino-1-cyclohexanecarboxylic acid methyl ester 
• 503167-50-8 (1S,2R)-2-amino-cyclohexanecarboxylic acid methyl ester 
• 501-53-1 benzyl chloroformate 
• 91259-90-4 (1S,6R)-6-Benzyloxycarbonylamino-cyclohex-3-ene-1-carboxylic acid methyl ester 
• 267230-45-5 (1R,2R)-2-aminocyclohexanecarboxylic acid methyl ester 
• 290838-42-5 methyl (1R,2R)-2-(((benzyloxy)carbonyl)amino)cyclohexane-1-carboxylate 

Downstream Products

• 290838-42-5 methyl (1R,2R)-2-(((benzyloxy)carbonyl)amino)cyclohexane-1-carboxylate 
• 5691-19-0 (1R,2R)-2-aminocyclohexanecarboxylic Acid 

Relevant articles and documents

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The present application describes modulators of CCR3 of formula (I): or pharmaceutically acceptable salt forms thereof, useful for the prevention of asthma and other allergic diseases.

1, 2-Disubstituted cyclohexane derived tripeptide aldehydes as novel selective thrombin inhibitors

A series of tripeptide arginine aldehydes was synthesized by replacement of proline with 1,2-disubstituted cyclohexane derivatives in the sequence of D-MePhe-Pro-Arg-H. Based on molecular modeling, further modification of the D-MePhe residue resulted in a potent and selective thrombin inhibitor.