Cas 126474-59-7,(1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-10-Benzyloxy-3a,5a-dimethyl-6-((R)-1,4,5-trimethyl-hexyl)-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalene

126474-59-7

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Basic information

Product Name: (1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-10-Benzyloxy-3a,5a-dimethyl-6-((R)-1,4,5-trimethyl-hexyl)-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalene
Synonyms:
CAS NO:126474-59-7
Molecular Formula:
Molecular Weight: 490.813
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: (1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-10-Benzyloxy-3a,5a-dimethyl-6-((R)-1,4,5-trimethyl-hexyl)-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalene(CAS DataBase Reference)
NIST Chemistry Reference: (1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-10-Benzyloxy-3a,5a-dimethyl-6-((R)-1,4,5-trimethyl-hexyl)-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalene(126474-59-7)
EPA Substance Registry System: (1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-10-Benzyloxy-3a,5a-dimethyl-6-((R)-1,4,5-trimethyl-hexyl)-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalene(126474-59-7)

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: 126474-59-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 126474-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,4,7 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 126474-59:
(8*1)+(7*2)+(6*6)+(5*4)+(4*7)+(3*4)+(2*5)+(1*9)=137
137 % 10 = 7
So 126474-59-7 is a valid CAS Registry Number.

126474-59-7Upstream product

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126474-59-7Relevant academic research and scientific papers

THE SYNTHESIS OF A 3,5-CYCLOSTEROIDAL ALDEHYDE FROM THE DISTILLATES OF CANOLA OIL

Neeland, Edward G.,Towers, G. H. N.

, p. 2603 - 2612 (2007/10/02)

Ozonolysis of an A,B-ring functionalized derivative of phytosterols found in the deodorizer distillate of canola oil gave the desired aldehyde 5.Canola oil thus provides a readily avaliable and inexpensive source of a key intermediate 5 which is frequently employed in steroidal synthesis.

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