Cas 1290145-58-2,8-(3-(benzylamino)-3-oxo-1-phenylpropyl)hexahydro-1,3,2-oxazaborolo[2,3-b]-1,3,2-oxazaborol-4-ium-8-uide

1290145-58-2

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Basic information

Product Name: 8-(3-(benzylamino)-3-oxo-1-phenylpropyl)hexahydro-1,3,2-oxazaborolo[2,3-b]-1,3,2-oxazaborol-4-ium-8-uide
Synonyms:
CAS NO:1290145-58-2
Molecular Formula:
Molecular Weight: 352.241
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: 8-(3-(benzylamino)-3-oxo-1-phenylpropyl)hexahydro-1,3,2-oxazaborolo[2,3-b]-1,3,2-oxazaborol-4-ium-8-uide(CAS DataBase Reference)
NIST Chemistry Reference: 8-(3-(benzylamino)-3-oxo-1-phenylpropyl)hexahydro-1,3,2-oxazaborolo[2,3-b]-1,3,2-oxazaborol-4-ium-8-uide(1290145-58-2)
EPA Substance Registry System: 8-(3-(benzylamino)-3-oxo-1-phenylpropyl)hexahydro-1,3,2-oxazaborolo[2,3-b]-1,3,2-oxazaborol-4-ium-8-uide(1290145-58-2)

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: 1290145-58-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1290145-58-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,0,1,4 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1290145-58:
(9*1)+(8*2)+(7*9)+(6*0)+(5*1)+(4*4)+(3*5)+(2*5)+(1*8)=142
142 % 10 = 2
So 1290145-58-2 is a valid CAS Registry Number.

1290145-58-2Upstream product

1290145-58-2Downstream Products

1290145-69-5 (3-(benzylamino)-3-oxo-1-phenylpropyl)boronic acid

1290145-58-2Relevant academic research and scientific papers

A method for the deprotection of alkylpinacolyl boronate esters

Sun, Jing,Perfetti, Michael T.,Santos, Webster L.

experimental part, p. 3571 - 3575 (2011/06/24)

A two-step procedure for deprotection of alkylpinacolyl boronate esters via transesterification with diethanolamine followed by hydrolysis was successfully developed with the advantages of tolerance to various functional groups, short reaction time, and ease of product isolation.

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