Cas 902141-73-5,di(isopropyl)carbamic acid (S)-1-(4,4,5,5-tetramethyl[1,3,2]-dioxaborolan-2-yl)-3-(3,4,5-trimethoxyphenyl)propyl ester

902141-73-5

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Basic information

Product Name: di(isopropyl)carbamic acid (S)-1-(4,4,5,5-tetramethyl[1,3,2]-dioxaborolan-2-yl)-3-(3,4,5-trimethoxyphenyl)propyl ester
Synonyms:
CAS NO:902141-73-5
Molecular Formula:
Molecular Weight: 479.422
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: di(isopropyl)carbamic acid (S)-1-(4,4,5,5-tetramethyl[1,3,2]-dioxaborolan-2-yl)-3-(3,4,5-trimethoxyphenyl)propyl ester(CAS DataBase Reference)
NIST Chemistry Reference: di(isopropyl)carbamic acid (S)-1-(4,4,5,5-tetramethyl[1,3,2]-dioxaborolan-2-yl)-3-(3,4,5-trimethoxyphenyl)propyl ester(902141-73-5)
EPA Substance Registry System: di(isopropyl)carbamic acid (S)-1-(4,4,5,5-tetramethyl[1,3,2]-dioxaborolan-2-yl)-3-(3,4,5-trimethoxyphenyl)propyl ester(902141-73-5)

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: 902141-73-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 902141-73-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,2,1,4 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 902141-73:
(8*9)+(7*0)+(6*2)+(5*1)+(4*4)+(3*1)+(2*7)+(1*3)=125
125 % 10 = 5
So 902141-73-5 is a valid CAS Registry Number.

902141-73-5Upstream product

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902141-73-5Relevant academic research and scientific papers

Synthesis of (S)-(-)-N-acetylcolchinol using intramolecular biaryl oxidative coupling

Besong, Gilbert,Jarowicki, Krzysztof,Kocienski, Philip J.,Sliwinski, Eric,Boyle, F. Thomas

, p. 2193 - 2207 (2006)

An asymmetric synthesis of the tubulin polymerisation inhibitor (S)-(-)-N-acetylcolchinol is reported based on an intramolecular biaryl oxidative coupling of a 1,3-diarylpropyl acetamide intermediate using phenyliodonium bis(trifluoroacetate) as the final

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