Cas 185944-56-3,Carbamic acid, [1-[[(4-methoxyphenyl)methoxy]methyl]-2-pentadecenyl]-, 1,1-dimethylethyl ester, (S)-

185944-56-3

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Basic information

Product Name: Carbamic acid, [1-[[(4-methoxyphenyl)methoxy]methyl]-2-pentadecenyl]-, 1,1-dimethylethyl ester, (S)-
Synonyms:
CAS NO:185944-56-3
Molecular Formula: C29H49NO4
Molecular Weight: 475.712
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: Carbamic acid, [1-[[(4-methoxyphenyl)methoxy]methyl]-2-pentadecenyl]-, 1,1-dimethylethyl ester, (S)-(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [1-[[(4-methoxyphenyl)methoxy]methyl]-2-pentadecenyl]-, 1,1-dimethylethyl ester, (S)-(185944-56-3)
EPA Substance Registry System: Carbamic acid, [1-[[(4-methoxyphenyl)methoxy]methyl]-2-pentadecenyl]-, 1,1-dimethylethyl ester, (S)-(185944-56-3)

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: 185944-56-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 185944-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,9,4 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 185944-56:
(8*1)+(7*8)+(6*5)+(5*9)+(4*4)+(3*4)+(2*5)+(1*6)=183
183 % 10 = 3
So 185944-56-3 is a valid CAS Registry Number.

185944-56-3Upstream product

185944-56-3Downstream Products

185944-56-3Relevant academic research and scientific papers

2-Aminoalcohol immunosuppressants: Structure-activity relationships

Hirose, Ryoji,Hamamichi, Norimitsu,Kitao, Yuuki,Matsuzaki, Tohru,Chiba, Kenji,Fujita, Tetsuro

, p. 2647 - 2650 (2007/10/03)

The 2-aminoalcohol series of immunosuppressants showed a bell-shaped relationship between the activity and the carbon number. The (R)-isomers were more potent than the (S)-isomers, and (R)-2-aminohexadecanol displayed comparably activity to a potent immunosuppressant, FTY720.

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