Cas 915377-91-2,2-(4-benzyloxy-3,3-dimethyl-cyclopent-1-enyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane

915377-91-2

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Basic information

Product Name: 2-(4-benzyloxy-3,3-dimethyl-cyclopent-1-enyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
Synonyms: 2-(4-benzyloxy-3,3-dimethyl-cyclopent-1-enyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
CAS NO:915377-91-2
Molecular Formula:
Molecular Weight: 328.259
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-(4-benzyloxy-3,3-dimethyl-cyclopent-1-enyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-benzyloxy-3,3-dimethyl-cyclopent-1-enyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(915377-91-2)
EPA Substance Registry System: 2-(4-benzyloxy-3,3-dimethyl-cyclopent-1-enyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(915377-91-2)

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: 915377-91-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 915377-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,3,7 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 915377-91:
(8*9)+(7*1)+(6*5)+(5*3)+(4*7)+(3*7)+(2*9)+(1*1)=192
192 % 10 = 2
So 915377-91-2 is a valid CAS Registry Number.

915377-91-2Upstream product

4058-51-9 2,2-dimethyl-3,4-pentadienal

915377-91-2Downstream Products

915377-93-4 4-(4-benzyloxy-3,3-dimethyl-cyclopent-1-enyl)-benzoic acid ethyl ester

915377-91-2Relevant academic research and scientific papers

Palladium-catalyzed asymmetric silaboration of allenes

Ohmura, Toshimichi,Taniguchi, Hiroki,Suginome, Michinori

, p. 13682 - 13683 (2006)

An enantioselective silaboration of allenes was achieved using an achiral silylborane in the presence of a palladium catalyst bearing a chiral monodentate phosphine ligand. (R)-2-Bis(3,5-dimethylphenyl)phosphino-1,1-binaphthyl gave the highest enantiosele

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