Cas 532402-38-3,2-[3-(<i>tert</i>-butyl-dimethyl-silanyloxy)-propenyl]-4,4,5,5-tetraphenyl-[1,3,2]dioxaborolane

532402-38-3

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Basic information

Product Name: 2-[3-(tert-butyl-dimethyl-silanyloxy)-propenyl]-4,4,5,5-tetraphenyl-[1,3,2]dioxaborolane
Synonyms:
CAS NO:532402-38-3
Molecular Formula:
Molecular Weight: 546.589
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: 2-[3-(tert-butyl-dimethyl-silanyloxy)-propenyl]-4,4,5,5-tetraphenyl-[1,3,2]dioxaborolane(CAS DataBase Reference)
NIST Chemistry Reference: 2-[3-(tert-butyl-dimethyl-silanyloxy)-propenyl]-4,4,5,5-tetraphenyl-[1,3,2]dioxaborolane(532402-38-3)
EPA Substance Registry System: 2-[3-(tert-butyl-dimethyl-silanyloxy)-propenyl]-4,4,5,5-tetraphenyl-[1,3,2]dioxaborolane(532402-38-3)

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: 532402-38-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 532402-38-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,2,4,0 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 532402-38:
(8*5)+(7*3)+(6*2)+(5*4)+(4*0)+(3*2)+(2*3)+(1*8)=113
113 % 10 = 3
So 532402-38-3 is a valid CAS Registry Number.

532402-38-3Upstream product

532402-38-3Downstream Products

532402-39-4 (E)-3-(4,4,5,5-Tetraphenyl-[1,3,2]dioxaborolan-2-yl)-prop-2-en-1-ol

532402-38-3Relevant academic research and scientific papers

1,1,2,2-Tetraphenyl-1,2-ethanediol: A new protecting group for the synthesis of cyclopropylboronic esters

Pietruszka, J?rg,Witt, Andreas

, p. 91 - 94 (2007/10/03)

While enantiomerically pure auxiliaries and protecting groups for boronic acids are well established, much less attention has been paid to achiral derivatives. The commercially available benzpinacol (9) proved to yield highly stable boronic esters. The ne

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