Cas 75731-87-2,(4-Bromo-phenyl)-carbamic acid (R)-3-methyl-2-((R)-1-methyl-pentyl)-cyclohex-1-enylmethyl ester

75731-87-2

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Basic information

Product Name: (4-Bromo-phenyl)-carbamic acid (R)-3-methyl-2-((R)-1-methyl-pentyl)-cyclohex-1-enylmethyl ester
Synonyms: (4-Bromo-phenyl)-carbamic acid (R)-3-methyl-2-((R)-1-methyl-pentyl)-cyclohex-1-enylmethyl ester
CAS NO:75731-87-2
Molecular Formula:
Molecular Weight: 408.379
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: (4-Bromo-phenyl)-carbamic acid (R)-3-methyl-2-((R)-1-methyl-pentyl)-cyclohex-1-enylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4-Bromo-phenyl)-carbamic acid (R)-3-methyl-2-((R)-1-methyl-pentyl)-cyclohex-1-enylmethyl ester(75731-87-2)
EPA Substance Registry System: (4-Bromo-phenyl)-carbamic acid (R)-3-methyl-2-((R)-1-methyl-pentyl)-cyclohex-1-enylmethyl ester(75731-87-2)

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: 75731-87-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 75731-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,3 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75731-87:
(7*7)+(6*5)+(5*7)+(4*3)+(3*1)+(2*8)+(1*7)=152
152 % 10 = 2
So 75731-87-2 is a valid CAS Registry Number.

75731-87-2Upstream product

75731-87-2Downstream Products

75731-87-2Relevant academic research and scientific papers

Regio- and stereochemistry of dialkylcuprate additions to selected alkyldene oxiranes

Ziegler, Frederick E.,Cady, Michael A.

, p. 122 - 128 (2007/10/02)

The stereochemistry of the vinyloxiranes obtained by the treatment of several alkylidene cyclohexanones with dimethylsulfonium methylide is discussed.The structure and stereochemistry of the products produced by treatment of the vinyloxiranes with lithium

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