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191480-69-0

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191480-69-0 Usage

General Description

The chemical compound "(1S,2R)-1-benzyloxy-2-(benzyloxymethyl)-3-cyclopentene" is a bicyclic organic compound consisting of a cyclopentene ring with benzyloxy and benzyloxymethyl groups attached to it. It is a chiral molecule with a stereocenter at the first and second position of the cyclopentene ring. (1S.2R)-1-Benzyloxy-2-(benzyloxymethyl)-3-cyclopentene is commonly used as a building block in organic synthesis and can be utilized in the preparation of various pharmaceuticals and natural products. Its structural features and functional groups make it a versatile intermediate in the production of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 191480-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,4,8 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 191480-69:
(8*1)+(7*9)+(6*1)+(5*4)+(4*8)+(3*0)+(2*6)+(1*9)=150
150 % 10 = 0
So 191480-69-0 is a valid CAS Registry Number.

191480-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S.2R)-1-Benzyloxy-2-(benzyloxymethyl)-3-cyclopentene

1.2 Other means of identification

Product number -
Other names Methyl 5-Acetamido-2,4,7,8,9-penta-O-acetyl-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosylonate N-Acetylneuraminic Acid Methyl Ester 2,4,7,8,9-Pentaacetate

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:191480-69-0 SDS

191480-69-0Relevant articles and documents

Preparation method of entecavir intermediate

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Paragraph 0031-0033; 0037-0039; 0043-0045, (2021/06/26)

The invention provides a preparation method of an entecavir intermediate, and particularly relates to a preparation method of (1S-(1[alpha], 2[alpha], 3[beta], 5[alpha])-2-((benzyloxy) methyl)-6-oxabicyclo [3.1. 0] hexyl-3-alcohol and an oxabicyclo compound (NT02). The invention provides a brand new preparation route and reaction process conditions, and has the advantages of high operation safety, simple method, low cost and high yield. The product yield is obviously improved, and the method is very suitable for industrial production and application.

Preparation method of oxa-dicyclohexane compound

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Paragraph 0023-0025; 0029-0031; 0035-0037, (2021/06/26)

The invention provides a preparation method of an entecavir intermediate, and particularly relates to a preparation method of an oxabicyclo [3.1.0] hexane compound (NT02). According to the preparation method, hydrogen peroxide is adopted as an oxygen source to replace tert-butyl hydroperoxide, the cost is low, the method is simple, the product yield is remarkably improved, and the preparation method is very suitable for industrial production and application.

PCSK9 INHIBITORS AND METHODS OF USE THEREOF

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Page/Page column 145; 146, (2020/07/31)

The invention relates to novel heteroaryl compounds and pharmaceutical preparations thereof. The invention further relates to methods of treating or preventing cardiovascular diseases, and methods treating sepsis or septic shock, using the novel heterocyclic compounds disclosed herein.

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