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654680-82-7

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  • (1R,3R,4S,6S)-4-Amino-4,7,7-trimethyl-bicyclo[4.1.0]hept-3-yl)-methanol

    Cas No: 654680-82-7

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654680-82-7 Usage

General Description

(1R,3R,4S,6S)-4-AMINO-4,7,7-TRIMETHYL-BICYCLO[4.1.0]HEPT-3-YL-METHANOL is a chemical compound with a bicyclic structure. It contains a hydroxyl group attached to a bicyclic heptane ring, with a methyl group at the 4th and 7th carbon positions. Additionally, it contains an amino group at the 4th carbon position. (1R,3R,4S,6S)-4-AMINO-4,7,7-TRIMETHYL-BICYCLO[4.1.0]HEPT-3-YL-METHANOL may have potential pharmaceutical applications due to its unique structure and functional groups, but further research is needed to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 654680-82-7 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, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 654680-82:
(8*6)+(7*5)+(6*4)+(5*6)+(4*8)+(3*0)+(2*8)+(1*2)=187
187 % 10 = 7
So 654680-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H21NO/c1-10(2)8-4-7(6-13)11(3,12)5-9(8)10/h7-9,13H,4-6,12H2,1-3H3/t7-,8+,9-,11-/m0/s1

654680-82-7SDS

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 (4-amino-4,7,7-trimethyl-3-bicyclo[4.1.0]heptanyl)methanol

1.2 Other means of identification

Product number -
Other names {(1R,3R,4S,6S)-4-amino-4,7,7-trimethylbicyclo[4.1.0]heptan-3-yl}methanol

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:654680-82-7 SDS

654680-82-7Relevant articles and documents

Synthesis of new chiral schiff bases from (+)-3-carene and their use in asymmetric oxidation of sulfides catalyzed by metal complexes

Koneva,Volcho,Korchagina,Salakhutdinov,To

experimental part, p. 815 - 824 (2009/12/09)

A number of new chiral Schiff bases were synthesized starting from accessible monoterpene (+)-3-carene, and the products were used as ligands in metal complex-catalyzed oxidation of sulfides to chiral sulfoxides. The optical purity and the sign of optical rotation of chiral sulfoxides were found to strongly depend on the oxidation temperature. Pleiades Publishing, Ltd., 2009.

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