Cas 1527477-66-2,(2E,4Z)-ethyl 5-(dimethylcarbamoyloxy)-5-phenyl-3-(prop-1-en-2-yl)penta-2,4-dienoate

1527477-66-2

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Basic information

Product Name: (2E,4Z)-ethyl 5-(dimethylcarbamoyloxy)-5-phenyl-3-(prop-1-en-2-yl)penta-2,4-dienoate
Synonyms: (2E,4Z)-ethyl 5-(dimethylcarbamoyloxy)-5-phenyl-3-(prop-1-en-2-yl)penta-2,4-dienoate
CAS NO:1527477-66-2
Molecular Formula:
Molecular Weight: 329.396
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: (2E,4Z)-ethyl 5-(dimethylcarbamoyloxy)-5-phenyl-3-(prop-1-en-2-yl)penta-2,4-dienoate(CAS DataBase Reference)
NIST Chemistry Reference: (2E,4Z)-ethyl 5-(dimethylcarbamoyloxy)-5-phenyl-3-(prop-1-en-2-yl)penta-2,4-dienoate(1527477-66-2)
EPA Substance Registry System: (2E,4Z)-ethyl 5-(dimethylcarbamoyloxy)-5-phenyl-3-(prop-1-en-2-yl)penta-2,4-dienoate(1527477-66-2)

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: 1527477-66-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1527477-66-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,2,7,4,7 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1527477-66:
(9*1)+(8*5)+(7*2)+(6*7)+(5*4)+(4*7)+(3*7)+(2*6)+(1*6)=192
192 % 10 = 2
So 1527477-66-2 is a valid CAS Registry Number.

1527477-66-2Upstream product

1527477-66-2Downstream Products

1527477-94-6 6-phenyl-4-(prop-1-en-2-yl)-2H-pyran-2-one

1527477-66-2Relevant academic research and scientific papers

Rh(III)-catalyzed C-H activation with allenes to synthesize conjugated olefins

Gong, Tian-Jun,Su, Wei,Liu, Zhao-Jing,Cheng, Wan-Min,Xiao, Bin,Fu, Yao

supporting information, p. 330 - 333 (2014/04/03)

RhIII-catalyzed C-H activation with allenes produces highly unsaturated conjugated olefins. The reaction is applicable to both olefin and arene C(sp2)-H and is compatible with a variety of functional groups. The products can be further transformed into ot

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