Cas 1095262-99-9,(1R,2S,3S,4S)-2-(l(-)-menthyl) 3-methyl 7-bis(methoxy)bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate

1095262-99-9

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Basic information

Product Name: (1R,2S,3S,4S)-2-(l(-)-menthyl) 3-methyl 7-bis(methoxy)bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate
Synonyms: (1R,2S,3S,4S)-2-(l(-)-menthyl) 3-methyl 7-bis(methoxy)bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate
CAS NO:1095262-99-9
Molecular Formula:
Molecular Weight: 394.508
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: (1R,2S,3S,4S)-2-(l(-)-menthyl) 3-methyl 7-bis(methoxy)bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S,3S,4S)-2-(l(-)-menthyl) 3-methyl 7-bis(methoxy)bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate(1095262-99-9)
EPA Substance Registry System: (1R,2S,3S,4S)-2-(l(-)-menthyl) 3-methyl 7-bis(methoxy)bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate(1095262-99-9)

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: 1095262-99-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1095262-99-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,5,2,6 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1095262-99:
(9*1)+(8*0)+(7*9)+(6*5)+(5*2)+(4*6)+(3*2)+(2*9)+(1*9)=169
169 % 10 = 9
So 1095262-99-9 is a valid CAS Registry Number.

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1095262-99-9Relevant academic research and scientific papers

Enantioselective synthesis of the carbocyclic D-ring subunit of massadine

Breder, Alexander,Chinigo, Gary M.,Waltman, Andrew W.,Carreira, Erick M.

supporting information; experimental part, p. 8514 - 8517 (2009/05/15)

(Chemical Equation Presented) Getting to the center of it: The strategy for an efficient asymmetric synthesis of the D-ring subunit embedded in massadine (1) includes: application of a cationic norbornyl rearrangement, ozonolytic cleavage displaying remar

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