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1H-Imidazole, 2-[(1S,2R,3S)-1,2,3-tris(phenylmethoxy)-4-(triphenylmethoxy)butyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

577995-58-5

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577995-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 577995-58-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,7,9,9 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 577995-58:
(8*5)+(7*7)+(6*7)+(5*9)+(4*9)+(3*5)+(2*5)+(1*8)=245
245 % 10 = 5
So 577995-58-5 is a valid CAS Registry Number.

577995-58-5SDS

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 2-[(1S,2R,3S)-1,2,3-tris(benzyloxy)-4-(trityloxy)butyl]-1H-imidazole

1.2 Other means of identification

Product number -
Other names 2-((1S,2R,3S)-1,2,3-Tris-benzyloxy-4-trityloxy-butyl)-1H-imidazole

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:577995-58-5 SDS

577995-58-5Relevant academic research and scientific papers

Synthesis of substituted imidazolo[1,2-α]piperidinoses and their evaluation as glycosidase inhibitors

Dubost, Estelle,Le Nouen, Didier,Streith, Jacques,Tarnus, Celine,Tschamber, Theophile

, p. 610 - 626 (2007/10/03)

The synthesis of substituted imidazolo[1,2-α]-L-arabino-piperidinoses is reported. The substituents are methyl, phenylmethyl, phenylethyl, cyclohexylethyl, pyridinylethyl, piperidinylethyl, phenylpropyl and hydroxymethyl. All substituents are connected to

Increasing the inhibitory potency of L-arabino-imidazolo-[1,2]-piperidinose towards β-D-glucosidase and β-D-galactosidase

Dubost, Estelle,Tschamber, Théophile,Streith, Jacques

, p. 3667 - 3670 (2007/10/03)

The synthesis of some potent inhibitors of two retaining β-glycosidases was achieved by introducing aglycon-mimics into the imidazole moiety of L-arabino azasugar 1. The strongest inhibition was observed with the phenyl-ethyl substituent at C(2) of 1 agai

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