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64431-71-6

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64431-71-6 Usage

General Description

1,7,7-trimethylbicyclo[2.2.1]hept-2-yl 5-oxo-DL-prolinate is a chemical compound that belongs to the class of bicyclic compounds. It has a bicyclo[2.2.1]heptane skeleton with a 5-oxo-DL-prolinate functional group attached to the 2-carbon of the bicyclo[2.2.1]heptane ring. The compound is a derivative of proline, an amino acid, and it is often used in pharmaceutical research and development. Its unique structure and functional group composition make it a potentially important compound for medicinal chemistry and drug design. Further studies on the compound's properties and potential applications could lead to new developments in the field of pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 64431-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,3 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64431-71:
(7*6)+(6*4)+(5*4)+(4*3)+(3*1)+(2*7)+(1*1)=116
116 % 10 = 6
So 64431-71-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H23NO3/c1-14(2)9-6-7-15(14,3)11(8-9)19-13(18)10-4-5-12(17)16-10/h9-11H,4-8H2,1-3H3,(H,16,17)

64431-71-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) 5-oxopyrrolidine-2-carboxylate

1.2 Other means of identification

Product number -
Other names EINECS 264-896-7

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:64431-71-6 SDS

64431-71-6Downstream Products

64431-71-6Relevant articles and documents

Method for the Direct Enantioselective Synthesis of Chiral Primary α-Amino Ketones by Catalytic α-Amination

Han, Yixin,Corey

supporting information, p. 283 - 286 (2019/01/10)

A useful catalytic enantioselective approach has been developed for the synthesis of chiral ketamine analogs using Rh(II)-catalyzed amination of triisopropylsilyl enol ethers to form α-amino ketones with O-(4-nitrophenyl)hydroxylamine as nitrogen donor in 81-91% ee.

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