Cas 303176-76-3,Dimethyl-carbamic acid (1S,2S,5R,6S)-5,6-bis-benzyloxy-4-benzyloxymethyl-2-chloro-cyclohex-3-enyl ester

303176-76-3

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Basic information

Product Name: Dimethyl-carbamic acid (1S,2S,5R,6S)-5,6-bis-benzyloxy-4-benzyloxymethyl-2-chloro-cyclohex-3-enyl ester
Synonyms: Dimethyl-carbamic acid (1S,2S,5R,6S)-5,6-bis-benzyloxy-4-benzyloxymethyl-2-chloro-cyclohex-3-enyl ester
CAS NO:303176-76-3
Molecular Formula:
Molecular Weight: 536.068
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: Dimethyl-carbamic acid (1S,2S,5R,6S)-5,6-bis-benzyloxy-4-benzyloxymethyl-2-chloro-cyclohex-3-enyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Dimethyl-carbamic acid (1S,2S,5R,6S)-5,6-bis-benzyloxy-4-benzyloxymethyl-2-chloro-cyclohex-3-enyl ester(303176-76-3)
EPA Substance Registry System: Dimethyl-carbamic acid (1S,2S,5R,6S)-5,6-bis-benzyloxy-4-benzyloxymethyl-2-chloro-cyclohex-3-enyl ester(303176-76-3)

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: 303176-76-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 303176-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,3,1,7 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 303176-76:
(8*3)+(7*0)+(6*3)+(5*1)+(4*7)+(3*6)+(2*7)+(1*6)=113
113 % 10 = 3
So 303176-76-3 is a valid CAS Registry Number.

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303176-76-3Relevant academic research and scientific papers

A new synthetic approach towards N-alkylated 2-epi-valienamines via palladium-catalyzed coupling reaction

Kok,Shing

, p. 6865 - 6868 (2000)

Preparation of N-alkylated 2-epi-valienamines was accomplished by the palladium-catalyzed coupling reaction of the allylic chloride 5 with various amines in the presence of trimethylolpropane phosphite (TMPP). The 2-epi-valienamine precursor (i.e. allylic

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