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(R)-(+)-1-AMINO-2-(METHOXYMETHYL)PYRROLIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72748-99-3

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72748-99-3 Usage

Chemical Properties

Colorless to light yellow liqui

Uses

Reagent for asymmetric synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 72748-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,4 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72748-99:
(7*7)+(6*2)+(5*7)+(4*4)+(3*8)+(2*9)+(1*9)=163
163 % 10 = 3
So 72748-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2O/c1-9-5-6-3-2-4-8(6)7/h6H,2-5,7H2,1H3/t6-/m1/s1

72748-99-3 Well-known Company Product Price

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  • Aldrich

  • (281581)  (R)-(+)-1-Amino-2-(methoxymethyl)pyrrolidine  96%

  • 72748-99-3

  • 281581-1G

  • 1,526.85CNY

  • Detail

72748-99-3SDS

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 (R)-(+)-1-AMINO-2-(METHOXYMETHYL)PYRROLIDINE

1.2 Other means of identification

Product number -
Other names (2R)-2-(methoxymethyl)pyrrolidin-1-amine

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:72748-99-3 SDS

72748-99-3Relevant academic research and scientific papers

ASYMMETRIC MICHAEL ADDITIONS VIA SAMP-/RAMP-HYDRAZONES ANTI-DIASTEREO- AND ENANTIOSELECTIVE SYNTHESIS OF 3,4-DISUBSTITUTED 5-OXO-ALKANOATES

Enders, Dieter,Papadopoulos, Kyriakos,Rendenbach, Beatrice E.M.,Appel, Rolf,Knoch, Falk

, p. 3491 - 3494 (2007/10/02)

An efficient and highly anti-diastereo-(de=90-100percent) and enantioselective (ee=92-100percent) synthesis of 3,4-disubstituted 5-oxo-alkanoates 3 in good overall chemical yields is described.The procedure involves the asymmetric Michael addition of aldehydes or ketones to enoates via their lithiated SAMP-/RAMP-hydrazones.Both enantiomers are accessible at will.

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