Cas 125995-55-3,Benzyl-carbamic acid (3S,4R,5S,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-20-oxa-cyclopropa[4,5]cyclopenta[a]phenanthren-3-yl ester

125995-55-3

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Basic information

Product Name: Benzyl-carbamic acid (3S,4R,5S,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-20-oxa-cyclopropa[4,5]cyclopenta[a]phenanthren-3-yl ester
Synonyms:
CAS NO:125995-55-3
Molecular Formula:
Molecular Weight: 535.811
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: Benzyl-carbamic acid (3S,4R,5S,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-20-oxa-cyclopropa[4,5]cyclopenta[a]phenanthren-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzyl-carbamic acid (3S,4R,5S,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-20-oxa-cyclopropa[4,5]cyclopenta[a]phenanthren-3-yl ester(125995-55-3)
EPA Substance Registry System: Benzyl-carbamic acid (3S,4R,5S,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-20-oxa-cyclopropa[4,5]cyclopenta[a]phenanthren-3-yl ester(125995-55-3)

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: 125995-55-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 125995-55-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,9,9 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 125995-55:
(8*1)+(7*2)+(6*5)+(5*9)+(4*9)+(3*5)+(2*5)+(1*5)=163
163 % 10 = 3
So 125995-55-3 is a valid CAS Registry Number.

125995-55-3Upstream product

119449-86-4 Benzyl-carbamic acid (3S,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

125995-55-3Downstream Products

125995-55-3Relevant academic research and scientific papers

Steric Control of Epoxidation by Carbamate and Amide Groups. Evidence for the Carbonyl-Directed Epoxidation

Kocovsky, Pavel,Stary, Ivo

, p. 3236 - 3243 (1990)

Allylic and homoallylic carbamoyloxy groups show a pronounced syn stereodirecting effect on peroxy acid epoxidation similar to that of hydroxy groups (5 -> 8).Carbonyl oxygen of the ambident carbamoyloxy group has been found to be responsible for this ste

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