Cas 1422557-41-2,3-[2-{[(1S)-1-(hydroxymethyl)-2,2-dimethylpropyl]amino}-2-oxoethyl]-1-cyclohexyl-1H-benzimidazolium chloride

1422557-41-2

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Basic information

Product Name: 3-[2-{[(1S)-1-(hydroxymethyl)-2,2-dimethylpropyl]amino}-2-oxoethyl]-1-cyclohexyl-1H-benzimidazolium chloride
Synonyms: 3-[2-{[(1S)-1-(hydroxymethyl)-2,2-dimethylpropyl]amino}-2-oxoethyl]-1-cyclohexyl-1H-benzimidazolium chloride
CAS NO:1422557-41-2
Molecular Formula:
Molecular Weight: 393.957
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: 3-[2-{[(1S)-1-(hydroxymethyl)-2,2-dimethylpropyl]amino}-2-oxoethyl]-1-cyclohexyl-1H-benzimidazolium chloride(CAS DataBase Reference)
NIST Chemistry Reference: 3-[2-{[(1S)-1-(hydroxymethyl)-2,2-dimethylpropyl]amino}-2-oxoethyl]-1-cyclohexyl-1H-benzimidazolium chloride(1422557-41-2)
EPA Substance Registry System: 3-[2-{[(1S)-1-(hydroxymethyl)-2,2-dimethylpropyl]amino}-2-oxoethyl]-1-cyclohexyl-1H-benzimidazolium chloride(1422557-41-2)

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: 1422557-41-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1422557-41-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,2,5,5 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1422557-41:
(9*1)+(8*4)+(7*2)+(6*2)+(5*5)+(4*5)+(3*7)+(2*4)+(1*1)=142
142 % 10 = 2
So 1422557-41-2 is a valid CAS Registry Number.

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1422557-41-2Relevant academic research and scientific papers

Highly tunable anionic tethered N-heterocyclic carbene of Pd(II) complexes for asymmetric allylic alkylation reaction

Shirasaki, Hiroshi,Kawakami, Miaki,Yamada, Haruka,Arakawa, Ryuichi,Sakaguchi, Satoshi

, p. 46 - 55 (2013/03/13)

The versatility of the anionic tethered NHC ligand system for the Pd-catalyzed allylic asymmetric alkylation (AAA) reaction was investigated. A well defined anionic amidate/NHC-Pd(II) complex catalyzed the AAA reaction of 1,3-diphenylprop-3-en-1-yl acetat

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