Cas 1535164-77-2,1-(4-(bromomethyl)-2,5-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N,N-trimethylmethanaminium bromide

1535164-77-2

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Basic information

Product Name: 1-(4-(bromomethyl)-2,5-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N,N-trimethylmethanaminium bromide
Synonyms:
CAS NO:1535164-77-2
Molecular Formula:
Molecular Weight: 574.997
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: 1-(4-(bromomethyl)-2,5-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N,N-trimethylmethanaminium bromide(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-(bromomethyl)-2,5-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N,N-trimethylmethanaminium bromide(1535164-77-2)
EPA Substance Registry System: 1-(4-(bromomethyl)-2,5-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-N,N,N-trimethylmethanaminium bromide(1535164-77-2)

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: 1535164-77-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1535164-77-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,3,5,1,6 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1535164-77:
(9*1)+(8*5)+(7*3)+(6*5)+(5*1)+(4*6)+(3*4)+(2*7)+(1*7)=162
162 % 10 = 2
So 1535164-77-2 is a valid CAS Registry Number.

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1535164-77-2Relevant academic research and scientific papers

The leaving group strongly affects H2O2-induced dna cross-linking by arylboronates

Cao, Sheng,Wang, Yibin,Peng, Xiaohua

, p. 501 - 508 (2014)

We evaluated the effects of the benzylic leaving group and core structure of arylboronates on H2O2-induced formation of bisquinone methides for DNA interstrand crosslinking. The mechanism of DNA cross-linking induced by these arylboronates involves genera

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