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99940-70-2

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99940-70-2 Usage

Chemical class

Piperazinediones

Molar mass

232.28 g/mol

Chiral center

One (which leads to two enantiomers, (R)and (S)-)

Physical form

White to light yellow solid

Potential applications

Pharmaceuticals and organic synthesis (due to unique structure and properties)

Need for further research

Yes (to explore potential uses and effects)

Check Digit Verification of cas no

The CAS Registry Mumber 99940-70-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,9,4 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 99940-70:
(7*9)+(6*9)+(5*9)+(4*4)+(3*0)+(2*7)+(1*0)=192
192 % 10 = 2
So 99940-70-2 is a valid CAS Registry Number.

99940-70-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (6R)-1-N-benzyl-6-methyl-piperazine-2,5-dione

1.2 Other means of identification

Product number -
Other names (R)-1-Benzyl-6-methyl-piperazine-2,5-dione

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:99940-70-2 SDS

99940-70-2Relevant articles and documents

Stereoselective synthesis of dipeptides - I

Favero, Valentina,Porzi, Gianni,Sandri, Sergio

, p. 599 - 612 (2007/10/03)

The alkylation of 7 occurs in moderate to good trans stereoselection (d.e.40-98%), while a poorer d.e. (40-98%) is observed for 8. On the contrary, in both substrates the alkylation with CH3I produces a greater amount of the cis isomer (d.e.48%).). Cleavage of the lactims 9(a,e) gives enantiomerically pure dipeptides 14(a,e). The absolute configuration of the introduced stereogenic centres has been assigned on the basis of the 1H-NMR data in connection with the conformational analysis.

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