Cas 83010-21-3,(3S,4R)-3-((E)-(S)-3-Cyclohexyl-3-hydroxy-propenyl)-4-hydroxy-2-(6-hydroxy-hexylsulfanyl)-cyclopentanone

83010-21-3

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Basic information

Product Name: (3S,4R)-3-((E)-(S)-3-Cyclohexyl-3-hydroxy-propenyl)-4-hydroxy-2-(6-hydroxy-hexylsulfanyl)-cyclopentanone
Synonyms:
CAS NO:83010-21-3
Molecular Formula:
Molecular Weight: 370.554
EINECS: N/A
Product Categories: N/A
Mol File: 83010-21-3.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (3S,4R)-3-((E)-(S)-3-Cyclohexyl-3-hydroxy-propenyl)-4-hydroxy-2-(6-hydroxy-hexylsulfanyl)-cyclopentanone(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4R)-3-((E)-(S)-3-Cyclohexyl-3-hydroxy-propenyl)-4-hydroxy-2-(6-hydroxy-hexylsulfanyl)-cyclopentanone(83010-21-3)
EPA Substance Registry System: (3S,4R)-3-((E)-(S)-3-Cyclohexyl-3-hydroxy-propenyl)-4-hydroxy-2-(6-hydroxy-hexylsulfanyl)-cyclopentanone(83010-21-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 83010-21-3(Hazardous Substances Data)

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(3S,4R)-3-((E)-(S)-3-Cyclohexyl-3-hydroxy-propenyl)-4-hydroxy-2-(6-hydroxy-hexylsulfanyl)-cyclopentanone
Cas No: 83010-21-3
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(3S,4R)-3-((E)-(S)-3-Cyclohexyl-3-hydroxy-propenyl)-4-hydroxy-2-(6-hydroxy-hexylsulfanyl)-cyclopentanone
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83010-21-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83010-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,1 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83010-21:
(7*8)+(6*3)+(5*0)+(4*1)+(3*0)+(2*2)+(1*1)=83
83 % 10 = 3
So 83010-21-3 is a valid CAS Registry Number.

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83010-21-3Relevant articles and documents

Synthesis of 7-thiaprostaglandin E1 congeners: Potent inhibitors of platelet aggregation

Tanaka,Okamura,Bannai,Hazato,Sugiura,Manabe,Kamimoto,Kurozumi

, p. 2359 - 2385 (1985)

Novel 7-thiaprostaglandin E1 derivatives and congeners were synthesized by a stepwise three-component coupling process, which involves the introduction of α-side chains (thiols) and β-side chains (organocopper reagents) into (R)-4-tert-butyldim

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