Cas 1186225-49-9,3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-p-tolylcyclohexanone

1186225-49-9

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Basic information

Product Name: 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-p-tolylcyclohexanone
Synonyms: 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-p-tolylcyclohexanone
CAS NO:1186225-49-9
Molecular Formula:
Molecular Weight: 314.233
EINECS: N/A
Product Categories: N/A
Mol File: 1186225-49-9.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: 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-p-tolylcyclohexanone(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-p-tolylcyclohexanone(1186225-49-9)
EPA Substance Registry System: 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-p-tolylcyclohexanone(1186225-49-9)

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: 1186225-49-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1186225-49-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,6,2,2 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1186225-49:
(9*1)+(8*1)+(7*8)+(6*6)+(5*2)+(4*2)+(3*5)+(2*4)+(1*9)=159
159 % 10 = 9
So 1186225-49-9 is a valid CAS Registry Number.

1186225-49-9Upstream product

1186225-49-9Downstream Products

1186225-49-9Relevant articles and documents

Catalytic asymmetric synthesis of chiral tertiary organoboronic esters through conjugate boration of β-substituted cyclic enones

Chen, I.-Hon,Yin, Liang,Itano, Wataru,Kanai, Motomu,Shibasaki, Masakatsu

supporting information; experimental part, p. 11664 - 11665 (2009/12/08)

(Chemical Equation Presented) The first catalytic enantioselective conjugate boration of β-substituted cyclic enones was developed to produce enantiomerically enriched tertiary organoboronates. The optimized asymmetric catalyst includes a QuinoxP*/s

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