Cas 404034-63-5,Carbamic acid, [2-[[2-(1-methylethenyl)-3-furanyl]ethynyl]phenyl]-, ethyl ester

404034-63-5

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Basic information

Product Name: Carbamic acid, [2-[[2-(1-methylethenyl)-3-furanyl]ethynyl]phenyl]-, ethyl ester
Synonyms:
CAS NO:404034-63-5
Molecular Formula: C18H17NO3
Molecular Weight: 295.338
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: Carbamic acid, [2-[[2-(1-methylethenyl)-3-furanyl]ethynyl]phenyl]-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [2-[[2-(1-methylethenyl)-3-furanyl]ethynyl]phenyl]-, ethyl ester(404034-63-5)
EPA Substance Registry System: Carbamic acid, [2-[[2-(1-methylethenyl)-3-furanyl]ethynyl]phenyl]-, ethyl ester(404034-63-5)

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: 404034-63-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 404034-63-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,4,0,3 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 404034-63:
(8*4)+(7*0)+(6*4)+(5*0)+(4*3)+(3*4)+(2*6)+(1*3)=95
95 % 10 = 5
So 404034-63-5 is a valid CAS Registry Number.

404034-63-5Upstream product

404034-63-5Downstream Products

404034-64-6 2-(2-isopropenylfuran-3-yl)indole

404034-63-5Relevant academic research and scientific papers

A concise synthesis of furostifoline by tetrabutylammonium fluoride-promoted indole ring formation.

Yasuhara, Akito,Suzuki, Naoyuki,Sakamoto, Takao

, p. 143 - 145 (2002)

Furostifoline, a furo[3,2-a]carbazole alkaloid, was synthesized in 10% overall yield in four steps from 2-acetyl-3-bromofuran. The key step of this synthesis was the 2-substituted indole formation with tetrabutylammonium fluoride (TBAF) from 2-(2-propenyl

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