Cas 75207-60-2,3-((3R,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-Hexamethyl-icosahydro-cyclopenta[a]chrysen-3-yl)-butyraldehyde

75207-60-2

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Basic information

Product Name: 3-((3R,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-Hexamethyl-icosahydro-cyclopenta[a]chrysen-3-yl)-butyraldehyde
Synonyms: 3-((3R,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-Hexamethyl-icosahydro-cyclopenta[a]chrysen-3-yl)-butyraldehyde
CAS NO:75207-60-2
Molecular Formula:
Molecular Weight: 440.753
EINECS: N/A
Product Categories: N/A

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: 3-((3R,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-Hexamethyl-icosahydro-cyclopenta[a]chrysen-3-yl)-butyraldehyde(CAS DataBase Reference)
NIST Chemistry Reference: 3-((3R,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-Hexamethyl-icosahydro-cyclopenta[a]chrysen-3-yl)-butyraldehyde(75207-60-2)
EPA Substance Registry System: 3-((3R,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-Hexamethyl-icosahydro-cyclopenta[a]chrysen-3-yl)-butyraldehyde(75207-60-2)

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: 75207-60-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 75207-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,0 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75207-60:
(7*7)+(6*5)+(5*2)+(4*0)+(3*7)+(2*6)+(1*0)=122
122 % 10 = 2
So 75207-60-2 is a valid CAS Registry Number.

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75207-60-2Relevant academic research and scientific papers

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

Bisseret, Philippe,Rohmer, Michel

, p. 7077 - 7080 (2007/10/02)

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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