Cas 212839-05-9,(2R,3R)-2-tert-Butoxycarbonylamino-15-methyl-3-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-hexadecanoic acid ethyl ester

212839-05-9

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Basic information

Product Name: (2R,3R)-2-tert-Butoxycarbonylamino-15-methyl-3-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-hexadecanoic acid ethyl ester
Synonyms:
CAS NO:212839-05-9
Molecular Formula:
Molecular Weight: 645.8
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: (2R,3R)-2-tert-Butoxycarbonylamino-15-methyl-3-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-hexadecanoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R)-2-tert-Butoxycarbonylamino-15-methyl-3-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-hexadecanoic acid ethyl ester(212839-05-9)
EPA Substance Registry System: (2R,3R)-2-tert-Butoxycarbonylamino-15-methyl-3-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-hexadecanoic acid ethyl ester(212839-05-9)

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: 212839-05-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 212839-05-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,8,3 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 212839-05:
(8*2)+(7*1)+(6*2)+(5*8)+(4*3)+(3*9)+(2*0)+(1*5)=119
119 % 10 = 9
So 212839-05-9 is a valid CAS Registry Number.

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212839-05-9Relevant academic research and scientific papers

An efficient synthesis of sulfobacin A (flavocristamide B), sulfobacin B, and flavocristamide A

Shioiri, Takayuki,Irako, Naoko

, p. 9129 - 9142 (2000)

Sulfobacin A (flavocristamide B, 1), sulfobacin B (2), and flavocristamide A (3), biologically active sulfonolipids, have been efficiently synthesized utilizing the asymmetric aldol reaction of the Schiff base 8 derived from glycine ester and (+)-2-hydroxy-3-pinanone (HyPN). (C) 2000 Elsevier Science Ltd.

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