Cas 1962-37-4,4-benzyl-2,3-dihydro-1H-inden-1-one

1962-37-4

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Basic information

Product Name: 4-benzyl-2,3-dihydro-1H-inden-1-one
Synonyms: 4-benzyl-2,3-dihydro-1H-inden-1-one
CAS NO:1962-37-4
Molecular Formula:
Molecular Weight: 222.287
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: 4-benzyl-2,3-dihydro-1H-inden-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 4-benzyl-2,3-dihydro-1H-inden-1-one(1962-37-4)
EPA Substance Registry System: 4-benzyl-2,3-dihydro-1H-inden-1-one(1962-37-4)

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: 1962-37-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1962-37-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,6 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1962-37:
(6*1)+(5*9)+(4*6)+(3*2)+(2*3)+(1*7)=94
94 % 10 = 4
So 1962-37-4 is a valid CAS Registry Number.

1962-37-4Upstream product

1962-37-4Downstream Products

56461-08-6 4-benzoylindan-1-one

1962-37-4Relevant academic research and scientific papers

The Dual Role of Benzophenone in Visible-Light/Nickel Photoredox-Catalyzed C?H Arylations: Hydrogen-Atom Transfer and Energy Transfer

Dewanji, Abhishek,Krach, Patricia E.,Rueping, Magnus

supporting information, p. 3566 - 3570 (2019/02/26)

A dual catalytic protocol for the direct arylation of non-activated C(sp3)?H bonds has been developed. Upon photochemical excitation, the excited triplet state of a diaryl ketone photosensitizer abstracts a hydrogen atom from an aliphatic C?H bond. This inherent reactivity was exploited for the generation of benzylic radicals which subsequently enter a nickel catalytic cycle, accomplishing the benzylic arylation.

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