Cas 169824-05-9,2-O-octadecyl-3-O-(phenylmethyl)-6-bromo-6-deoxy-L-ascorbic acid

169824-05-9

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Basic information

Product Name: 2-O-octadecyl-3-O-(phenylmethyl)-6-bromo-6-deoxy-L-ascorbic acid
Synonyms: 2-O-octadecyl-3-O-(phenylmethyl)-6-bromo-6-deoxy-L-ascorbic acid
CAS NO:169824-05-9
Molecular Formula:
Molecular Weight: 581.631
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: 2-O-octadecyl-3-O-(phenylmethyl)-6-bromo-6-deoxy-L-ascorbic acid(CAS DataBase Reference)
NIST Chemistry Reference: 2-O-octadecyl-3-O-(phenylmethyl)-6-bromo-6-deoxy-L-ascorbic acid(169824-05-9)
EPA Substance Registry System: 2-O-octadecyl-3-O-(phenylmethyl)-6-bromo-6-deoxy-L-ascorbic acid(169824-05-9)

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: 169824-05-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 169824-05-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,8,2 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 169824-05:
(8*1)+(7*6)+(6*9)+(5*8)+(4*2)+(3*4)+(2*0)+(1*5)=169
169 % 10 = 9
So 169824-05-9 is a valid CAS Registry Number.

169824-05-9Upstream product

98829-11-9 2-O-octadecyl-3-O-benzyl-ascorbic acid

169824-05-9Downstream Products

169824-05-9Relevant academic research and scientific papers

Cardioselective ammonium, phosphonium, and sulfonium analogues of α- tocopherol and ascorbic acid that inhibit in vitro and ex vivo lipid peroxidation and scavenge superoxide radicals

Grisar,Marciniak,Bolkenius,Verne-Mismer,Wagner

, p. 2880 - 2886 (1995)

Analogues of α-tocopherol and ascorbic acid with permanently cationic substituents, i.e., phosphonium (8, 9), sulfonium (11), acylhydrazinium (13, 14), and ammonium (1, 16, 21), were synthesized, and the 2R and 2S enantiomers of the α-tocopherol analogues

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