Cas 87828-62-4,(1′R,2′S,5′R,2E,4E)-2′-isopropyl-5′-methylcyclohex-1′-yl 5-phenylpenta-2,4-dienoate

87828-62-4

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Basic information

Product Name: (1′R,2′S,5′R,2E,4E)-2′-isopropyl-5′-methylcyclohex-1′-yl 5-phenylpenta-2,4-dienoate
Synonyms: (1′R,2′S,5′R,2E,4E)-2′-isopropyl-5′-methylcyclohex-1′-yl 5-phenylpenta-2,4-dienoate
CAS NO:87828-62-4
Molecular Formula:
Molecular Weight: 312.452
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: (1′R,2′S,5′R,2E,4E)-2′-isopropyl-5′-methylcyclohex-1′-yl 5-phenylpenta-2,4-dienoate(CAS DataBase Reference)
NIST Chemistry Reference: (1′R,2′S,5′R,2E,4E)-2′-isopropyl-5′-methylcyclohex-1′-yl 5-phenylpenta-2,4-dienoate(87828-62-4)
EPA Substance Registry System: (1′R,2′S,5′R,2E,4E)-2′-isopropyl-5′-methylcyclohex-1′-yl 5-phenylpenta-2,4-dienoate(87828-62-4)

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: 87828-62-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 87828-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,2 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87828-62:
(7*8)+(6*7)+(5*8)+(4*2)+(3*8)+(2*6)+(1*2)=184
184 % 10 = 4
So 87828-62-4 is a valid CAS Registry Number.

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87828-62-4Relevant academic research and scientific papers

Preparation of conjugated dienoates with Bestmann ylide: Towards the synthesis of zampanolide and dactylolide using a facile linchpin approach

Wang, Jingjing,Ting, Samuel Z. Y.,Harvey, Joanne E.

supporting information, p. 1815 - 1822 (2016/04/10)

Bestmann ylide [(triphenylphosphoranylidene)ketene] acts as a chemical linchpin that links nucleophilic entities, such as alcohols or amines, with carbonyl moieties to produce unsaturated esters and amides, respectively. In this work, the formation of α,β

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