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(1R,3R,4S,6S)-4-TERT-BUTOXYCARBONYLAMINO-4,7,7-TRIMETHYL-BICYCLO[4.1.0]HEPTANE-3-CARBOXYLIC ACID is a bicyclic compound with a carboxylic acid functional group. It features a tert-butoxycarbonylamino group at the carbon in position 4 and three methyl groups at the carbon in position 7. The molecule exhibits a specific stereochemistry, characterized by the R configuration at positions 1 and 3, and the S configuration at positions 4 and 6.

654680-62-3

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654680-62-3 Usage

Uses

Used in Organic Synthesis:
(1R,3R,4S,6S)-4-TERT-BUTOXYCARBONYLAMINO-4,7,7-TRIMETHYL-BICYCLO[4.1.0]HEPTANE-3-CARBOXYLIC ACID is used as a building block in organic synthesis for the creation of various organic compounds.
Used in Pharmaceutical Preparation:
(1R,3R,4S,6S)-4-TERT-BUTOXYCARBONYLAMINO-4,7,7-TRIMETHYL-BICYCLO[4.1.0]HEPTANE-3-CARBOXYLIC ACID is used as a starting material for the preparation of pharmaceuticals, potentially contributing to the development of new drugs and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 654680-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,4,6,8 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 654680-62:
(8*6)+(7*5)+(6*4)+(5*6)+(4*8)+(3*0)+(2*6)+(1*2)=183
183 % 10 = 3
So 654680-62-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H27NO4/c1-14(2,3)21-13(20)17-16(6)8-11-9(15(11,4)5)7-10(16)12(18)19/h9-11H,7-8H2,1-6H3,(H,17,20)(H,18,19)/t9-,10+,11+,16+/m1/s1

654680-62-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,3R,4S,6S)-4-TERT-BUTOXYCARBONYLAMINO-4,7,7-TRIMETHYL-BICYCLO[4.1.0]HEPTANE-3-CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names -

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

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More Details:654680-62-3 SDS

654680-62-3Relevant academic research and scientific papers

Synthesis and transformation of novel cyclic β-amino acid derivatives from (+)-3-carene

Gyonfalvi, Szilvia,Szakonyi, Zsolt,Fueloep, Ferenc

, p. 3965 - 3972 (2007/10/03)

The regio- and stereoselective addition of chlorosulfonyl isocyanate to (+)-3-carene 1 resulted in β-lactam 2, which was converted to N-Boc-β-amino acid 4, β-amino ester 7, and carboxamide derivatives 18 and 20 via N-Boc activation and mild ring opening.

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