Cas 849592-46-7,Carbamic acid, [(1S)-1-(1-acetyl-6-bromo-1H-indol-3-yl)-2-oxo-2-[(4R)-2-oxo-4-phenyl- 3-oxazolidinyl]ethyl]-, 1,1-dimethylethyl ester

849592-46-7

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Basic information

Product Name: Carbamic acid, [(1S)-1-(1-acetyl-6-bromo-1H-indol-3-yl)-2-oxo-2-[(4R)-2-oxo-4-phenyl- 3-oxazolidinyl]ethyl]-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:849592-46-7
Molecular Formula: C26H26BrN3O6
Molecular Weight: 556.413
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: Carbamic acid, [(1S)-1-(1-acetyl-6-bromo-1H-indol-3-yl)-2-oxo-2-[(4R)-2-oxo-4-phenyl- 3-oxazolidinyl]ethyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [(1S)-1-(1-acetyl-6-bromo-1H-indol-3-yl)-2-oxo-2-[(4R)-2-oxo-4-phenyl- 3-oxazolidinyl]ethyl]-, 1,1-dimethylethyl ester(849592-46-7)
EPA Substance Registry System: Carbamic acid, [(1S)-1-(1-acetyl-6-bromo-1H-indol-3-yl)-2-oxo-2-[(4R)-2-oxo-4-phenyl- 3-oxazolidinyl]ethyl]-, 1,1-dimethylethyl ester(849592-46-7)

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: 849592-46-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 849592-46-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,5,9 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 849592-46:
(8*8)+(7*4)+(6*9)+(5*5)+(4*9)+(3*2)+(2*4)+(1*6)=227
227 % 10 = 7
So 849592-46-7 is a valid CAS Registry Number.

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849592-46-7Relevant academic research and scientific papers

Total synthesis of marine bisindole alkaloids, (+)-hamacanthins A, B and (-)-antipode of 0cis-dihydrohamacanthin B

Kouko, Takashi,Matsumura, Ken,Kawasaki, Tomomi

, p. 2309 - 2318 (2007/10/03)

The total synthesis of the marine bisindole alkaloids, (+)-hamacanthins A (2a) and B (2b), and (-)-antipode of cis-dihydrohamacanthin B (2e) was achieved by transamidation-cyclization of N-(2-aminoethyl)-2-oxoethanamide 18 derived from (S)-indolylglycinol 10.

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