Cas 1395472-67-9,(1-benzyl-2-hydroxy-4-phenyl-2-(phenylethynyl)-but-3-ynyl)carbamic acid tert-butyl ester

1395472-67-9

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Basic information

Product Name: (1-benzyl-2-hydroxy-4-phenyl-2-(phenylethynyl)-but-3-ynyl)carbamic acid tert-butyl ester
Synonyms: (1-benzyl-2-hydroxy-4-phenyl-2-(phenylethynyl)-but-3-ynyl)carbamic acid tert-butyl ester
CAS NO:1395472-67-9
Molecular Formula:
Molecular Weight: 451.565
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: (1-benzyl-2-hydroxy-4-phenyl-2-(phenylethynyl)-but-3-ynyl)carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1-benzyl-2-hydroxy-4-phenyl-2-(phenylethynyl)-but-3-ynyl)carbamic acid tert-butyl ester(1395472-67-9)
EPA Substance Registry System: (1-benzyl-2-hydroxy-4-phenyl-2-(phenylethynyl)-but-3-ynyl)carbamic acid tert-butyl ester(1395472-67-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1395472-67-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1395472-67-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,5,4,7 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1395472-67:
(9*1)+(8*3)+(7*9)+(6*5)+(5*4)+(4*7)+(3*2)+(2*6)+(1*7)=199
199 % 10 = 9
So 1395472-67-9 is a valid CAS Registry Number.

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1395472-67-9Relevant academic research and scientific papers

Poly(ethylene glycol) as a reaction matrix in platinum- or gold-catalyzed cycloisomerization: A mechanistic investigation

Spina, Rosella,Colacino, Evelina,Martinez, Jean,Lamaty, Frédéric

, p. 3817 - 3821 (2013)

Design for diversity: A new catalytic system based on PEG-3400 and a metal salt (Pt or Au) was designed to efficiently perform a cycloisomerization reaction under microwave irradiation, which gave diverse heterocycles in good to excellent yields, after a

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