Cas 1070894-22-2,benzyl (6-(3,3-dimethyl-6-oxocyclohex-1-en-1-yl)benzo[d][1,3]dioxol-5-ylmethyl)carbamate

1070894-22-2

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Basic information

Product Name: benzyl (6-(3,3-dimethyl-6-oxocyclohex-1-en-1-yl)benzo[d][1,3]dioxol-5-ylmethyl)carbamate
Synonyms: benzyl (6-(3,3-dimethyl-6-oxocyclohex-1-en-1-yl)benzo[d][1,3]dioxol-5-ylmethyl)carbamate
CAS NO:1070894-22-2
Molecular Formula:
Molecular Weight: 407.466
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 (6-(3,3-dimethyl-6-oxocyclohex-1-en-1-yl)benzo[d][1,3]dioxol-5-ylmethyl)carbamate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl (6-(3,3-dimethyl-6-oxocyclohex-1-en-1-yl)benzo[d][1,3]dioxol-5-ylmethyl)carbamate(1070894-22-2)
EPA Substance Registry System: benzyl (6-(3,3-dimethyl-6-oxocyclohex-1-en-1-yl)benzo[d][1,3]dioxol-5-ylmethyl)carbamate(1070894-22-2)

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: 1070894-22-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1070894-22-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,0,8,9 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1070894-22:
(9*1)+(8*0)+(7*7)+(6*0)+(5*8)+(4*9)+(3*4)+(2*2)+(1*2)=152
152 % 10 = 2
So 1070894-22-2 is a valid CAS Registry Number.

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1070894-22-2Relevant academic research and scientific papers

Suzuki cross-coupling/reductive debenzyloxycarbonylation sequence for the syntheses of [c]annulated isoquinolines: Application for the syntheses of pancratistatin-like isoquinolines

Pandey, Ganesh,Balakrishnan, Madhesan

, p. 8128 - 8131 (2008/12/22)

(Chemical Equation Presented) A two-step strategy involving Suzuki cross-coupling of boronic acids with a diverse array of α-iodoenones followed by hydrogenation is developed for the construction of [c]annulated isoquinolines. This mild and efficient proc

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