Cas 883908-40-5,methyl (S)-(-)-2-((E)-2-acetyl-3-(phenylamino)but-2-enethioylamino)-4-methylpentanoate

883908-40-5

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Basic information

Product Name: methyl (S)-(-)-2-((E)-2-acetyl-3-(phenylamino)but-2-enethioylamino)-4-methylpentanoate
Synonyms: methyl (S)-(-)-2-((E)-2-acetyl-3-(phenylamino)but-2-enethioylamino)-4-methylpentanoate
CAS NO:883908-40-5
Molecular Formula:
Molecular Weight: 362.493
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: methyl (S)-(-)-2-((E)-2-acetyl-3-(phenylamino)but-2-enethioylamino)-4-methylpentanoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (S)-(-)-2-((E)-2-acetyl-3-(phenylamino)but-2-enethioylamino)-4-methylpentanoate(883908-40-5)
EPA Substance Registry System: methyl (S)-(-)-2-((E)-2-acetyl-3-(phenylamino)but-2-enethioylamino)-4-methylpentanoate(883908-40-5)

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: 883908-40-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 883908-40-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,9,0 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 883908-40:
(8*8)+(7*8)+(6*3)+(5*9)+(4*0)+(3*8)+(2*4)+(1*0)=215
215 % 10 = 5
So 883908-40-5 is a valid CAS Registry Number.

883908-40-5Upstream product

883908-40-5Downstream Products

883908-45-0 methyl (S)-(-)-4-methyl-2-((Z)-3-(phenylamino)but-2-enethioylamino)pentanoate

883908-40-5Relevant academic research and scientific papers

Synthesis of optically active isothiazole derivatives from L-(α)-amino acids

Ciez, Dariusz,Szneler

, p. 2059 - 2066 (2005)

Several enantiomerically pure 3,5-disubstituted isothiazol-5-ylideneamine hydrobromides were prepared by oxidation of chiral 3-amino-2,3-unsaturated thioamides. The starting thioamides derived from natural L-α-amino acids represent a novel group of synthe

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