Cas 149366-14-3,(R)-3-(3-Hydroxy-2-hydroxymethyl-propylsulfanyl)-2-(2,2,2-trichloro-ethoxycarbonylamino)-propionic acid tert-butyl ester

149366-14-3

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Basic information

Product Name: (R)-3-(3-Hydroxy-2-hydroxymethyl-propylsulfanyl)-2-(2,2,2-trichloro-ethoxycarbonylamino)-propionic acid tert-butyl ester
Synonyms:
CAS NO:149366-14-3
Molecular Formula:
Molecular Weight: 440.773
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: (R)-3-(3-Hydroxy-2-hydroxymethyl-propylsulfanyl)-2-(2,2,2-trichloro-ethoxycarbonylamino)-propionic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3-(3-Hydroxy-2-hydroxymethyl-propylsulfanyl)-2-(2,2,2-trichloro-ethoxycarbonylamino)-propionic acid tert-butyl ester(149366-14-3)
EPA Substance Registry System: (R)-3-(3-Hydroxy-2-hydroxymethyl-propylsulfanyl)-2-(2,2,2-trichloro-ethoxycarbonylamino)-propionic acid tert-butyl ester(149366-14-3)

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: 149366-14-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 149366-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,3,6 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 149366-14:
(8*1)+(7*4)+(6*9)+(5*3)+(4*6)+(3*6)+(2*1)+(1*4)=153
153 % 10 = 3
So 149366-14-3 is a valid CAS Registry Number.

149366-14-3Upstream product

98303-79-8 N-<<(2,2,2-trichloroethyl)oxy>carbonyl>-L-cysteine tert-butyl ester

149366-14-3Downstream Products

149366-14-3Relevant academic research and scientific papers

Structure-activity relationship of lipopeptide from outer membrane of Escherichia coli and synthesis of highly immunopotenting lipopeptide derivatives with an achiral lipo-part

Kurimura,Achiwa

, p. 627 - 629 (1993)

For outstanding the structure-activity relationship of lipopeptide derivatives, high biologically active lipopeptide derivatives with an achiral lipo-part were newly synthesized.

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