Cas 838864-68-9,Carbamic acid, [(3S,4S,5S)-tetrahydro-4-hydroxy-5-tetradecyl-3-furanyl]-, 1,1-dimethylethyl ester

838864-68-9

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Basic information

Product Name: Carbamic acid, [(3S,4S,5S)-tetrahydro-4-hydroxy-5-tetradecyl-3-furanyl]-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:838864-68-9
Molecular Formula: C23H45NO4
Molecular Weight: 399.615
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, [(3S,4S,5S)-tetrahydro-4-hydroxy-5-tetradecyl-3-furanyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [(3S,4S,5S)-tetrahydro-4-hydroxy-5-tetradecyl-3-furanyl]-, 1,1-dimethylethyl ester(838864-68-9)
EPA Substance Registry System: Carbamic acid, [(3S,4S,5S)-tetrahydro-4-hydroxy-5-tetradecyl-3-furanyl]-, 1,1-dimethylethyl ester(838864-68-9)

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: 838864-68-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 838864-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,8,8,6 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 838864-68:
(8*8)+(7*3)+(6*8)+(5*8)+(4*6)+(3*4)+(2*6)+(1*8)=229
229 % 10 = 9
So 838864-68-9 is a valid CAS Registry Number.

838864-68-9Upstream product

1453202-89-5 (3S,4S,5R)-4-(benzyloxy)-5-((R)-1-iodotetradecyl) tetrahydrofuran-3-ylcarbamate

838864-68-9Downstream Products

838864-68-9Relevant academic research and scientific papers

Stereoselective total synthesis of Jaspine B (Pachastrissamine) utilizing iodocyclization and an investigation of its cytotoxic activity

Ghosal, Partha,Ajay, Sama,Meena, Sanjeev,Sinha, Sudhir,Shaw, Arun K.

, p. 903 - 908 (2013/09/23)

The stereoselective synthesis of Jaspine B has been achieved from easily available (S)-Garner's aldehyde. The trisubstituted tetrahydrofuran core of Jaspine B was constructed by utilizing a diastereoselective iodocyclization as the key step. Deiodination

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