Cas 110611-20-6,2-((3S,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-Hexamethyl-icosahydro-cyclopenta[a]chrysen-3-yl)-propionic acid

110611-20-6

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Basic information

Product Name: 2-((3S,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-Hexamethyl-icosahydro-cyclopenta[a]chrysen-3-yl)-propionic acid
Synonyms: 2-((3S,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-Hexamethyl-icosahydro-cyclopenta[a]chrysen-3-yl)-propionic acid
CAS NO:110611-20-6
Molecular Formula:
Molecular Weight: 442.726
EINECS: N/A
Product Categories: N/A
Mol File: 110611-20-6.mol
Article Data: 1

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: 2-((3S,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-Hexamethyl-icosahydro-cyclopenta[a]chrysen-3-yl)-propionic acid(CAS DataBase Reference)
NIST Chemistry Reference: 2-((3S,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-Hexamethyl-icosahydro-cyclopenta[a]chrysen-3-yl)-propionic acid(110611-20-6)
EPA Substance Registry System: 2-((3S,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-Hexamethyl-icosahydro-cyclopenta[a]chrysen-3-yl)-propionic acid(110611-20-6)

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: 110611-20-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 110611-20-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,6,1 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 110611-20:
(8*1)+(7*1)+(6*0)+(5*6)+(4*1)+(3*1)+(2*2)+(1*0)=56
56 % 10 = 6
So 110611-20-6 is a valid CAS Registry Number.

110611-20-6Upstream product

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110611-20-6Relevant articles and documents

From Bio- to Geohopanoids: an Efficient Abiotic Passage Promoted by Oxygen in the Presence of Cuprous Chloride

Bisseret, Philippe,Rohmer, Michel

, p. 7077 - 7080 (1995)

In the presence of cuprous chloride, the representative biohopanoid 1a was smoothly converted by oxidation in pyridine into aldehydes, ketones and carboxylic acids with the same skeletons as those of molecular fossils ubiquitously found in the organic mat

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