Cas 1262642-47-6,N-tert-butyl ((5-acetyl-2-(pyridin-2-yl)phenyl)(phenyl)methyl)carbamate

1262642-47-6

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Basic information

Product Name: N-tert-butyl ((5-acetyl-2-(pyridin-2-yl)phenyl)(phenyl)methyl)carbamate
Synonyms: N-tert-butyl ((5-acetyl-2-(pyridin-2-yl)phenyl)(phenyl)methyl)carbamate
CAS NO:1262642-47-6
Molecular Formula:
Molecular Weight: 402.493
EINECS: N/A
Product Categories: N/A
Mol File: 1262642-47-6.mol
Article Data: 1

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: N-tert-butyl ((5-acetyl-2-(pyridin-2-yl)phenyl)(phenyl)methyl)carbamate(CAS DataBase Reference)
NIST Chemistry Reference: N-tert-butyl ((5-acetyl-2-(pyridin-2-yl)phenyl)(phenyl)methyl)carbamate(1262642-47-6)
EPA Substance Registry System: N-tert-butyl ((5-acetyl-2-(pyridin-2-yl)phenyl)(phenyl)methyl)carbamate(1262642-47-6)

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: 1262642-47-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1262642-47-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,6,4 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1262642-47:
(9*1)+(8*2)+(7*6)+(6*2)+(5*6)+(4*4)+(3*2)+(2*4)+(1*7)=146
146 % 10 = 6
So 1262642-47-6 is a valid CAS Registry Number.

1262642-47-6Upstream product

1262642-47-6Downstream Products

1262642-47-6Relevant articles and documents

Rhodium(III)-catalyzed arylation of Boc-imines via C-H bond functionalization

Tsai, Andy S.,Tauchert, Michael E.,Bergman, Robert G.,Ellman, Jonathan A.

, p. 1248 - 1250 (2011/04/16)

The first rhodium-catalyzed arylation of imines proceeding via C-H bond functionalization is reported. Use of a non-coordinating halide abstractor is important to obtain reactivity. Aryl-branched N-Boc-amines are formed, and a wide range of functionality is compatible with the reaction.

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