Cas 612836-13-2,dimethylphenyl-[(1S)-1-(2-phenylethyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl]silane

612836-13-2

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Basic information

Product Name: dimethylphenyl-[(1S)-1-(2-phenylethyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl]silane
Synonyms: dimethylphenyl-[(1S)-1-(2-phenylethyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl]silane
CAS NO:612836-13-2
Molecular Formula:
Molecular Weight: 406.448
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: dimethylphenyl-[(1S)-1-(2-phenylethyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl]silane(CAS DataBase Reference)
NIST Chemistry Reference: dimethylphenyl-[(1S)-1-(2-phenylethyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl]silane(612836-13-2)
EPA Substance Registry System: dimethylphenyl-[(1S)-1-(2-phenylethyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl]silane(612836-13-2)

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: 612836-13-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 612836-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,2,8,3 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 612836-13:
(8*6)+(7*1)+(6*2)+(5*8)+(4*3)+(3*6)+(2*1)+(1*3)=142
142 % 10 = 2
So 612836-13-2 is a valid CAS Registry Number.

612836-13-2Upstream product

1270304-75-0 (R)-dimethyl(phenyl)(3-phenyl-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propyl)silane

612836-13-2Downstream Products

612836-13-2Relevant academic research and scientific papers

Vinylidenation of Organoboronic Esters Enabled by a Pd-Catalyzed Metallate Shift

Aparece, Mark D.,Gao, Chenpeng,Lovinger, Gabriel J.,Morken, James P.

, p. 592 - 595 (2019)

Organoboron “ate” complexes undergo a net vinyl insertion reaction to give 1,1-disubstituted alkenyl boronic esters when treated with stoichiometric allyl acetate and a palladium catalyst. Reactions that employ vinyllithium afforded good to excellent yields after one hour, while reactions that employ vinylmagnesium chloride furnished modest to good yields after 18 hours.

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