Cas 1160791-33-2,4-chloro-6-(2-chlorophenyl)-3-(1,3-dithiolan-2-ylidene)-3,6-dihydro-2H-pyran-2-one

1160791-33-2

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Basic information

Product Name: 4-chloro-6-(2-chlorophenyl)-3-(1,3-dithiolan-2-ylidene)-3,6-dihydro-2H-pyran-2-one
Synonyms: 4-chloro-6-(2-chlorophenyl)-3-(1,3-dithiolan-2-ylidene)-3,6-dihydro-2H-pyran-2-one
CAS NO:1160791-33-2
Molecular Formula:
Molecular Weight: 345.27
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: 4-chloro-6-(2-chlorophenyl)-3-(1,3-dithiolan-2-ylidene)-3,6-dihydro-2H-pyran-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 4-chloro-6-(2-chlorophenyl)-3-(1,3-dithiolan-2-ylidene)-3,6-dihydro-2H-pyran-2-one(1160791-33-2)
EPA Substance Registry System: 4-chloro-6-(2-chlorophenyl)-3-(1,3-dithiolan-2-ylidene)-3,6-dihydro-2H-pyran-2-one(1160791-33-2)

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: 1160791-33-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1160791-33-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,7,9 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1160791-33:
(9*1)+(8*1)+(7*6)+(6*0)+(5*7)+(4*9)+(3*1)+(2*3)+(1*3)=142
142 % 10 = 2
So 1160791-33-2 is a valid CAS Registry Number.

1160791-33-2Upstream product

133294-44-7 C₁₄H₁₁ClO₃S₂

1160791-33-2Downstream Products

1160791-33-2Relevant academic research and scientific papers

Direct synthesis of polyfunctionalized unsaturated δ-lactones and δ-lactams from α-alkenoyl α-carboxyl/carbamoyl ketene S,S-acetals under Vilsmeier conditions

Liu, Jun,Wang, Mang,Han, Feng,Liu, Yingjie,Liu, Qun

, p. 5090 - 5092 (2009)

(Chemical Equation Presented) An efficient method for direct synthesis of polyfunctionalized unsaturated δ-lactones 2 and δ-lactams 4 has been developed from the reaction of the easily available α-alkenoyl α-carboxyl/carbamoyl ketene S,S-acetals 1/3 and V

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