Cas 874141-07-8,1-O-methoxymethyl-2-O-(13-(4-benzoylphenyl)-9-(Z)-tridecenyl)-sn-glycerol

874141-07-8

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Basic information

Product Name: 1-O-methoxymethyl-2-O-(13-(4-benzoylphenyl)-9-(Z)-tridecenyl)-sn-glycerol
Synonyms: 1-O-methoxymethyl-2-O-(13-(4-benzoylphenyl)-9-(Z)-tridecenyl)-sn-glycerol
CAS NO:874141-07-8
Molecular Formula:
Molecular Weight: 496.687
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-O-methoxymethyl-2-O-(13-(4-benzoylphenyl)-9-(Z)-tridecenyl)-sn-glycerol(CAS DataBase Reference)
NIST Chemistry Reference: 1-O-methoxymethyl-2-O-(13-(4-benzoylphenyl)-9-(Z)-tridecenyl)-sn-glycerol(874141-07-8)
EPA Substance Registry System: 1-O-methoxymethyl-2-O-(13-(4-benzoylphenyl)-9-(Z)-tridecenyl)-sn-glycerol(874141-07-8)

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: 874141-07-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 874141-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,1,4 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 874141-07:
(8*8)+(7*7)+(6*4)+(5*1)+(4*4)+(3*1)+(2*0)+(1*7)=168
168 % 10 = 8
So 874141-07-8 is a valid CAS Registry Number.

874141-07-8Upstream product

1027646-81-6 2-O-(13-(4-benzoylphenyl)-9-(Z)-tridecenyl)-3-O-(4-methoxyphenyl)-sn-glycerol

874141-07-8Downstream Products

874141-07-8Relevant academic research and scientific papers

Synthesis of photoactivatable analogues of lysophosphatidic acid and covalent labeling of plasma proteins

Li, Zaiguo,Baker, Daniel L.,Tigyi, Gabor,Bittman, Robert

, p. 629 - 635 (2007/10/03)

Lysophosphatidic acids hearing a benzophenone group in either the sn-1 or sn-2 chain of an oleoyl-type ester or oleyl-type ether chain and 32P in the phosphate group were synthesized. The benzophenone moiety was introduced by selective hydrobor

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