Cas 1360002-12-5,(E)-1-(4-bromophenyl)-2-methoxy-2-oxoethyl 4-(3-methoxy-3-oxoprop-1-en-1-yl)benzoate

1360002-12-5

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Basic information

Product Name: (E)-1-(4-bromophenyl)-2-methoxy-2-oxoethyl 4-(3-methoxy-3-oxoprop-1-en-1-yl)benzoate
Synonyms: (E)-1-(4-bromophenyl)-2-methoxy-2-oxoethyl 4-(3-methoxy-3-oxoprop-1-en-1-yl)benzoate
CAS NO:1360002-12-5
Molecular Formula:
Molecular Weight: 433.255
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: (E)-1-(4-bromophenyl)-2-methoxy-2-oxoethyl 4-(3-methoxy-3-oxoprop-1-en-1-yl)benzoate(CAS DataBase Reference)
NIST Chemistry Reference: (E)-1-(4-bromophenyl)-2-methoxy-2-oxoethyl 4-(3-methoxy-3-oxoprop-1-en-1-yl)benzoate(1360002-12-5)
EPA Substance Registry System: (E)-1-(4-bromophenyl)-2-methoxy-2-oxoethyl 4-(3-methoxy-3-oxoprop-1-en-1-yl)benzoate(1360002-12-5)

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: 1360002-12-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1360002-12-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,0,0 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1360002-12:
(9*1)+(8*3)+(7*6)+(6*0)+(5*0)+(4*0)+(3*2)+(2*1)+(1*2)=85
85 % 10 = 5
So 1360002-12-5 is a valid CAS Registry Number.

1360002-12-5Upstream product

1360002-12-5Downstream Products

1360002-12-5Relevant academic research and scientific papers

N-heterocyclic carbene-mediated hydroacylation-Sonogashira/Heck/Suzuki coupling in a single pot: A new cascade reaction

Sreenivasulu,Kumar, K. Siva,Kumar, P. Rajender,Chandrasekhar,Pal, Manojit

experimental part, p. 1670 - 1679 (2012/03/22)

A dually NHC-catalyzed reaction cascade comprising an initial hydroacylation of an activated ketone and subsequent Sonogashira/Heck/Suzuki coupling in the same pot is reported. The reaction mechanism and scope of the methodology is presented.

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