Cas 245484-08-6,(2S,3S,4S)-2-Hydroxymethyl-1-(4-methoxy-benzyl)-pyrrolidine-3,4-diol

245484-08-6

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Basic information

Product Name: (2S,3S,4S)-2-Hydroxymethyl-1-(4-methoxy-benzyl)-pyrrolidine-3,4-diol
Synonyms: (2S,3S,4S)-2-Hydroxymethyl-1-(4-methoxy-benzyl)-pyrrolidine-3,4-diol
CAS NO:245484-08-6
Molecular Formula:
Molecular Weight: 253.298
EINECS: N/A
Product Categories: N/A
Mol File: 245484-08-6.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2S,3S,4S)-2-Hydroxymethyl-1-(4-methoxy-benzyl)-pyrrolidine-3,4-diol(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,4S)-2-Hydroxymethyl-1-(4-methoxy-benzyl)-pyrrolidine-3,4-diol(245484-08-6)
EPA Substance Registry System: (2S,3S,4S)-2-Hydroxymethyl-1-(4-methoxy-benzyl)-pyrrolidine-3,4-diol(245484-08-6)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 245484-08-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 245484-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,4,8 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 245484-08:
(8*2)+(7*4)+(6*5)+(5*4)+(4*8)+(3*4)+(2*0)+(1*8)=146
146 % 10 = 6
So 245484-08-6 is a valid CAS Registry Number.

245484-08-6Upstream product

245484-08-6Downstream Products

52019-89-3 (2S,3S,4S)-2-(hydroxymethyl)pyrrolidine-3,4-diol

245484-08-6Relevant articles and documents

Novel and versatile synthesis of pyrrolidine type azasugars, DAB-1 and LAB-1, potent glucosidase inhibitors

Kim, Yong Jip,Kido, Masaru,Bando, Masahiko,Kitahara, Takeshi

, p. 7501 - 7508 (2007/10/03)

Synthesis or glucosidase inhibitors, DAB-1 (1) and LAB-1 (2) from diethyl tartrate is described. The procedure afforded an epimerizable mixture of diastereomeric intermediates 8 and ent. 8, and opened the door not only to the selective synthesis or DAB-1 and LAB-1 but for giving various related analogs.

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