Cas 921927-86-8,(2S,4R)-2-Methyl-4-((R)-2-methyl-propane-2-sulfinylamino)-5-phenyl-pentanoic acid methyl ester

921927-86-8

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Basic information

Product Name: (2S,4R)-2-Methyl-4-((R)-2-methyl-propane-2-sulfinylamino)-5-phenyl-pentanoic acid methyl ester
Synonyms: (2S,4R)-2-Methyl-4-((R)-2-methyl-propane-2-sulfinylamino)-5-phenyl-pentanoic acid methyl ester
CAS NO:921927-86-8
Molecular Formula:
Molecular Weight: 325.472
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: (2S,4R)-2-Methyl-4-((R)-2-methyl-propane-2-sulfinylamino)-5-phenyl-pentanoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,4R)-2-Methyl-4-((R)-2-methyl-propane-2-sulfinylamino)-5-phenyl-pentanoic acid methyl ester(921927-86-8)
EPA Substance Registry System: (2S,4R)-2-Methyl-4-((R)-2-methyl-propane-2-sulfinylamino)-5-phenyl-pentanoic acid methyl ester(921927-86-8)

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: 921927-86-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 921927-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,1,9,2 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 921927-86:
(8*9)+(7*2)+(6*1)+(5*9)+(4*2)+(3*7)+(2*8)+(1*6)=188
188 % 10 = 8
So 921927-86-8 is a valid CAS Registry Number.

921927-86-8Upstream product

921927-86-8Downstream Products

921927-98-2 desacetyl tubulysin D

921927-86-8Relevant academic research and scientific papers

The total synthesis of tubulysin D

Peltier, Hillary M.,McMahon, Jeffrey P.,Patterson, Andrew W.,Ellman, Jonathan A.

, p. 16018 - 16019 (2006)

The first total synthesis of tubulysin D is reported. The development and application of new tert-butanesulfinamide methods allowed for rapid syntheses of the tubuvaline and tubuphenylalanine fragments. Most significantly, a route was devised and implemen

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