Cas 1190069-69-2,(4S)-N-((1S,2R)-2-hydroxy-1-indanyl)-5,5-dimethyl-3-(2-benzyloxirane-2-carbonyl)thiazolidine-4-carboxamide

1190069-69-2

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Basic information

Product Name: (4S)-N-((1S,2R)-2-hydroxy-1-indanyl)-5,5-dimethyl-3-(2-benzyloxirane-2-carbonyl)thiazolidine-4-carboxamide
Synonyms:
CAS NO:1190069-69-2
Molecular Formula:
Molecular Weight: 452.574
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: (4S)-N-((1S,2R)-2-hydroxy-1-indanyl)-5,5-dimethyl-3-(2-benzyloxirane-2-carbonyl)thiazolidine-4-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: (4S)-N-((1S,2R)-2-hydroxy-1-indanyl)-5,5-dimethyl-3-(2-benzyloxirane-2-carbonyl)thiazolidine-4-carboxamide(1190069-69-2)
EPA Substance Registry System: (4S)-N-((1S,2R)-2-hydroxy-1-indanyl)-5,5-dimethyl-3-(2-benzyloxirane-2-carbonyl)thiazolidine-4-carboxamide(1190069-69-2)

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: 1190069-69-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1190069-69-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,0,6 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1190069-69:
(9*1)+(8*1)+(7*9)+(6*0)+(5*0)+(4*6)+(3*9)+(2*6)+(1*9)=152
152 % 10 = 2
So 1190069-69-2 is a valid CAS Registry Number.

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1190069-69-2Relevant academic research and scientific papers

α-Substituted norstatines as the transition-state mimic in inhibitors of multiple digestive vacuole malaria aspartic proteases

Orrling, Kristina M.,Marzahn, Melissa R.,Gutierrez-de-Teran, Hugo,Aqvist, Johan,Dunn, Ben M.,Larhed, Mats

experimental part, p. 5933 - 5949 (2009/12/24)

The impact of moving the P1 side-chain from the β-position to the α-position in norstatine-containing plasmepsin inhibitors was investigated, generating two new classes of tertiary alcohol-comprising α-benzylnorstatines and α-phenylnorstatines. Twelve α-s

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