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sodium (5R)-5-fluoro-5-{(3aS,4R,5R,6aS)-5-hydroxy-4-[(1Z,3S)-3-hydroxyoct-1-en-1-yl]-4,5,6,6a-tetrahydro-3aH-cyclopenta[b]furan-3-yl}pentanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

101641-82-1

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101641-82-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101641-82-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,6,4 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 101641-82:
(8*1)+(7*0)+(6*1)+(5*6)+(4*4)+(3*1)+(2*8)+(1*2)=81
81 % 10 = 1
So 101641-82-1 is a valid CAS Registry Number.

101641-82-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,(5R)-5-[(3aS,4R,5R,6aS)-5-hydroxy-4-[(Z,3S)-3-hydroxyoct-1-enyl]-4,5,6,6a-tetrahydro-3aH-cyclopenta[b]furan-3-yl]-5-fluoropentanoate

1.2 Other means of identification

Product number -
Other names Prosta-6,13-dien-1-oic acid,6,9-epoxy-5-fluoro-11,15-dihydroxy-,monosodium salt,(5S,9alpha,11alpha,13E,15S)

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:101641-82-1 SDS

101641-82-1Upstream product

101641-82-1Downstream Products

101641-82-1Relevant academic research and scientific papers

Synthesis of 5-Fluoroprostacyclin

Djuric, Stevan W.,Garland, Robert B.,Nysted, Leonard D.,Pappo, Raphael,Plume, Gatis,Swenton, Lydia

, p. 978 - 990 (2007/10/02)

Protected prostacyclin derivatives were reacted with perchloryl fluoride in methanol.The resultant 5-fluoro-6-methoxy derivatives were separated and identified.Pyrolysis of the individual isomers in the presence of magnesium triflate led to 5(R)- or 5(S)-

Method for preparing 5-fluoroprostacyclins

-

, (2008/06/13)

This invention relates to a process for preparing 5-fluoroprostacyclins that are useful for the treatment of platelet dysfunction.

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