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55516-35-3

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55516-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55516-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,5,1 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55516-35:
(7*5)+(6*5)+(5*5)+(4*1)+(3*6)+(2*3)+(1*5)=123
123 % 10 = 3
So 55516-35-3 is a valid CAS Registry Number.

55516-35-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name benzoic acid (3aR,4R,5R,6aS)-4-((E)-(R)-3-hydroxy-5-phenyl-pent-1-enyl)-2-oxo-hexahydro-cyclopenta[b]furan-5-yl ester

1.2 Other means of identification

Product number -
Other names (3aR,4R,5R,6aS)-4-[3R-hydroxy-5-phenyl-1E-pentenyl]-5-(benzoyloxy)-hexahydro-2H-cyclopenta[b]furan-2-one

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:55516-35-3 SDS

55516-35-3Downstream Products

55516-35-3Relevant articles and documents

PREPARATION OF PROSTAGLANDIN DERIVATIVES

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Page/Page column 19, (2012/02/05)

A process for preparing the prostaglandin derivatives is provided, wherein the benzoyl and p-nitrobenzoyl groups are used as the hydroxyl protective groups. A pharmaceutical composition comprising the prostaglandin derivatives is also provided.

Improved Process for the Production of Prostaglandins and Prostaglandin Analogs

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Page/Page column 54, (2010/01/29)

The present invention relates to an improved process for the production of prostaglandins and prostaglandin analogs. In particular, this invention relates to the production of prostaglandins of the PGF2α-series, including latanoprost, travoprost, and bimatoprost, which are active pharmaceutical ingredients used for the reduction of elevated intraocular pressure in patients with glaucoma and ocular hypertension.

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