Cas 1558764-09-2,(Z)-methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hex-1-enyl)benzoate

1558764-09-2

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Basic information

Product Name: (Z)-methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hex-1-enyl)benzoate
Synonyms: (Z)-methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hex-1-enyl)benzoate
CAS NO:1558764-09-2
Molecular Formula:
Molecular Weight: 344.259
EINECS: N/A
Product Categories: N/A
Mol File: 1558764-09-2.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: (Z)-methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hex-1-enyl)benzoate(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hex-1-enyl)benzoate(1558764-09-2)
EPA Substance Registry System: (Z)-methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hex-1-enyl)benzoate(1558764-09-2)

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: 1558764-09-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1558764-09-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,5,8,7,6 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1558764-09:
(9*1)+(8*5)+(7*5)+(6*8)+(5*7)+(4*6)+(3*4)+(2*0)+(1*9)=212
212 % 10 = 2
So 1558764-09-2 is a valid CAS Registry Number.

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1558764-09-2Relevant articles and documents

Ligand-free hydroboration of alkynes catalyzed by heterogeneous copper powder with high efficiency

Zhao, Jie,Niu, Zhiqiang,Fu, Hua,Li, Yadong

supporting information, p. 2058 - 2060 (2014/03/21)

Regioselective hydroboration of terminal and internal alkynes is realized by using 10 mol% copper powder (0.3-1 μm) at room temperature. 24 alkynes were efficiently converted into vinylboronates in up to 96% yield without addition of any ligand or additiv

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