Cas 1202183-67-2,(3aR,7aS)-ethyl 2,2-dimethyl-7-(4-nitrobenzoyloxy)-3a,6,7,7a-tetrahydrobenzo[d][1,3]dioxole-5-carboxylate

1202183-67-2

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Basic information

Product Name: (3aR,7aS)-ethyl 2,2-dimethyl-7-(4-nitrobenzoyloxy)-3a,6,7,7a-tetrahydrobenzo[d][1,3]dioxole-5-carboxylate
Synonyms: (3aR,7aS)-ethyl 2,2-dimethyl-7-(4-nitrobenzoyloxy)-3a,6,7,7a-tetrahydrobenzo[d][1,3]dioxole-5-carboxylate
CAS NO:1202183-67-2
Molecular Formula:
Molecular Weight: 391.378
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: (3aR,7aS)-ethyl 2,2-dimethyl-7-(4-nitrobenzoyloxy)-3a,6,7,7a-tetrahydrobenzo[d][1,3]dioxole-5-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,7aS)-ethyl 2,2-dimethyl-7-(4-nitrobenzoyloxy)-3a,6,7,7a-tetrahydrobenzo[d][1,3]dioxole-5-carboxylate(1202183-67-2)
EPA Substance Registry System: (3aR,7aS)-ethyl 2,2-dimethyl-7-(4-nitrobenzoyloxy)-3a,6,7,7a-tetrahydrobenzo[d][1,3]dioxole-5-carboxylate(1202183-67-2)

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: 1202183-67-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1202183-67-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,2,1,8 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1202183-67:
(9*1)+(8*2)+(7*0)+(6*2)+(5*1)+(4*8)+(3*3)+(2*6)+(1*7)=102
102 % 10 = 2
So 1202183-67-2 is a valid CAS Registry Number.

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1202183-67-2Relevant academic research and scientific papers

A concise route to (-)-shikimic acid and (-)-5-epi-shikimic acid, and their enantiomers via Barbier reaction and ring-closing metathesis

Kancharla, Pavan K.,Doddi, Venkata Ramana,Kokatla, Hariprasad,Vankar, Yashwant D.

, p. 6951 - 6954 (2009)

A simple route for the synthesis of naturally occurring (-)-shikimic acid, (-)-5-epi-shikimic acid, and their enantiomers from d-ribose-derived enantiomeric aldehydes 8a and 8b by employing Barbier reaction and ring-closing metathesis as key steps has bee

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