Cas 186754-00-7,N-tetradecanoyl-O-(3,4,6-tri-O-acetyl-2-deoxy-2-tetradecanoylamino-β-D-glucopyranosyl)-L-serine benzyl ester

186754-00-7

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Basic information

Product Name: N-tetradecanoyl-O-(3,4,6-tri-O-acetyl-2-deoxy-2-tetradecanoylamino-β-D-glucopyranosyl)-L-serine benzyl ester
Synonyms:
CAS NO:186754-00-7
Molecular Formula:
Molecular Weight: 903.207
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: N-tetradecanoyl-O-(3,4,6-tri-O-acetyl-2-deoxy-2-tetradecanoylamino-β-D-glucopyranosyl)-L-serine benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N-tetradecanoyl-O-(3,4,6-tri-O-acetyl-2-deoxy-2-tetradecanoylamino-β-D-glucopyranosyl)-L-serine benzyl ester(186754-00-7)
EPA Substance Registry System: N-tetradecanoyl-O-(3,4,6-tri-O-acetyl-2-deoxy-2-tetradecanoylamino-β-D-glucopyranosyl)-L-serine benzyl ester(186754-00-7)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 186754-00-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 186754-00-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,7,5 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 186754-00:
(8*1)+(7*8)+(6*6)+(5*7)+(4*5)+(3*4)+(2*0)+(1*0)=167
167 % 10 = 7
So 186754-00-7 is a valid CAS Registry Number.

186754-00-7Upstream product

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186754-00-7Relevant academic research and scientific papers

Lipid A and related compounds. XXXI. Synthesis of biologically active N-acylated L-serine-containing D-glucosamine 4-phosphate derivatives of lipid A

Miyajima, Keisuke,Ikeda, Kiyoshi,Achiwa, Kazuo

, p. 2268 - 2273 (1996)

New N-acylated L-serine-containing non-phosphorylated and phosphorylated D-glucosamine derivatives structurally corresponding to the lipid A disaccharide backbone were synthesized. Compounds 2, 4 and 5 exhibited potent mitogenic activity. Further, compound 5 showed nitric oxide (NO) productivity.

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