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1(2H)-Pyridinecarboxylic acid, 3,4-dihydro-3,4-dihydroxy-2-[(phenylmethoxy)methyl]-, phenylmethyl ester, (2R,3R,4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

389092-28-8

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389092-28-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 389092-28-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,0,9 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 389092-28:
(8*3)+(7*8)+(6*9)+(5*0)+(4*9)+(3*2)+(2*2)+(1*8)=188
188 % 10 = 8
So 389092-28-8 is a valid CAS Registry Number.

389092-28-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl (2R,3R,4R)-2-((benzyloxy)methyl)-3,4-dihydroxy-3,4-dihydropyridine-1(2H)-carboxylate

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:389092-28-8 SDS

389092-28-8Relevant academic research and scientific papers

Enantiopure 2,3-dihydro-4-pyridones as synthetic intermediates: Asymmetric synthesis of 1-deoxynojirimycin

Comins, Daniel L,Fulp, Alan B

, p. 6839 - 6841 (2007/10/03)

An asymmetric synthesis of 1-deoxynojirimycin (2) mediated by a chiral auxiliary is reported. The dihydropyridone 4 was converted to diol 11 in three steps by acetoxylation, hydrolysis, and stereoselective reduction. Dihydroxylation of 11 followed by catalytic reduction afforded 2.

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