Cas 1346757-25-2,butyl (2E,6E)-7-(2-chlorophenyl)-4-(1,3-dithiolan-2-ylidene)-5-oxohepta-2,6-dienoate

1346757-25-2

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Basic information

Product Name: butyl (2E,6E)-7-(2-chlorophenyl)-4-(1,3-dithiolan-2-ylidene)-5-oxohepta-2,6-dienoate
Synonyms: butyl (2E,6E)-7-(2-chlorophenyl)-4-(1,3-dithiolan-2-ylidene)-5-oxohepta-2,6-dienoate
CAS NO:1346757-25-2
Molecular Formula:
Molecular Weight: 408.97
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: butyl (2E,6E)-7-(2-chlorophenyl)-4-(1,3-dithiolan-2-ylidene)-5-oxohepta-2,6-dienoate(CAS DataBase Reference)
NIST Chemistry Reference: butyl (2E,6E)-7-(2-chlorophenyl)-4-(1,3-dithiolan-2-ylidene)-5-oxohepta-2,6-dienoate(1346757-25-2)
EPA Substance Registry System: butyl (2E,6E)-7-(2-chlorophenyl)-4-(1,3-dithiolan-2-ylidene)-5-oxohepta-2,6-dienoate(1346757-25-2)

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: 1346757-25-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1346757-25-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,6,7,5 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1346757-25:
(9*1)+(8*3)+(7*4)+(6*6)+(5*7)+(4*5)+(3*7)+(2*2)+(1*5)=182
182 % 10 = 2
So 1346757-25-2 is a valid CAS Registry Number.

1346757-25-2Upstream product

141-32-2 acrylic acid n-butyl ester

1346757-25-2Downstream Products

1346757-25-2Relevant academic research and scientific papers

Tandem [5+1] annulation-isocyanide cyclization: Efficient synthesis of hydroindolones

Wang, He,Zhao, Yu-Long,Ren, Chuan-Qing,Diallo, Aboubacar,Liu, Qun

, p. 12316 - 12318 (2011)

A new strategy for the rapid construction of functionalized reduced indoles starting from activated methylene isocyanides and 1,5-dielectrophilic 5-oxohepta-2,6-dienoates (and their equivalents) through a [5+1] annulation-isocyanide cyclization cascade un

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