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172016-60-3

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  • (1R,2S,3R,5S,δZ)-2-(tert-Butyldiphenylsilyloxy)methyl-5-hydroxy-3-tetrahydropyranyloxy-cyclopentanehept-δ-en-oic Acid Methyl Ester (Mixture of Diastereomers)

    Cas No: 172016-60-3

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  • (1R,2S,3R,5S,δZ)-2-(tert-Butyldiphenylsilyloxy)methyl-5-hydroxy-3-tetrahydropyranyloxy-cyclopentanehept-δ-en-oic Acid Methyl Ester (Mixture of Diastereomers)

    Cas No: 172016-60-3

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  • (1R,2S,3R,5S,δZ)-2-(tert-Butyldiphenylsilyloxy)methyl-5-hydroxy-3-tetrahydropyranyloxy-cyclopentanehept-δ-en-oic Acid Methyl Ester (Mixture of Diastereomers)

    Cas No: 172016-60-3

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172016-60-3 Usage

Uses

Intermediate in the production of Limaprost.

Check Digit Verification of cas no

The CAS Registry Mumber 172016-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,0,1 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 172016-60:
(8*1)+(7*7)+(6*2)+(5*0)+(4*1)+(3*6)+(2*6)+(1*0)=103
103 % 10 = 3
So 172016-60-3 is a valid CAS Registry Number.

172016-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (Z)-7-[(1R,2S,3R,5S)-2-[[tert-butyl(diphenyl)silyl]oxymethyl]-5-hydroxy-3-(oxan-2-yloxy)cyclopentyl]hept-5-enoate

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

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

More Details:172016-60-3 SDS

172016-60-3Downstream Products

172016-60-3Relevant articles and documents

Synthesis of (±)-15-deoxy-Δ12,14-prostaglandin J2 and Δ12-prostaglandin J2 15-acetate methyl esters

Vostrikov, N. S.,Lobko, I. F.,Miftakhov, M. S.,Ishimova, D. U.

, p. 1 - 9 (2015/03/18)

A new synthetic approach to 15-deoxy-Δ12,14-prostaglandin J2 and related compounds starting from Corey (±)-lactone diol has been developed. The key stage of this approach includes synthesis of a prostaglandin derivative possessing le

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