Cas 959760-78-2,(4-((1-decyloxycarbonyl-1-methylethyl)carbamoyl)phenyl)acetylene

959760-78-2

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Basic information

Product Name: (4-((1-decyloxycarbonyl-1-methylethyl)carbamoyl)phenyl)acetylene
Synonyms: (4-((1-decyloxycarbonyl-1-methylethyl)carbamoyl)phenyl)acetylene
CAS NO:959760-78-2
Molecular Formula:
Molecular Weight: 371.52
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-((1-decyloxycarbonyl-1-methylethyl)carbamoyl)phenyl)acetylene(CAS DataBase Reference)
NIST Chemistry Reference: (4-((1-decyloxycarbonyl-1-methylethyl)carbamoyl)phenyl)acetylene(959760-78-2)
EPA Substance Registry System: (4-((1-decyloxycarbonyl-1-methylethyl)carbamoyl)phenyl)acetylene(959760-78-2)

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: 959760-78-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 959760-78-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,9,7,6 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 959760-78:
(8*9)+(7*5)+(6*9)+(5*7)+(4*6)+(3*0)+(2*7)+(1*8)=242
242 % 10 = 2
So 959760-78-2 is a valid CAS Registry Number.

959760-78-2Upstream product

959760-78-2Downstream Products

959760-78-2Relevant academic research and scientific papers

Two-dimensional helix-bundle formation of a dynamic helical poly(phenylacetylene) with achiral pendant groups on graphite

Sakurai, Shin-Ichiro,Ohsawa, Sousuke,Nagai, Kanji,Okoshi, Kento,Kumaki, Jiro,Yashima, Eiji

, p. 7605 - 7608 (2007)

(Chemical Equation Presented) It all makes sense: A dynamically racemic helical polymer crystallizes on graphite upon exposure to an organic solvent vapor, resulting in two-dimensional helix-bundle formation. The enantiomeric right-and left-handed helical

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