Cas 689283-27-0,1-(RS<sub>S</sub>)-[5-N-methylcarbonyloxy-2-methyl-(2S,3Z)-3-pentenylsulfinyl]-benzene

689283-27-0

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Basic information

Product Name: 1-(RS_S)-[5-N-methylcarbonyloxy-2-methyl-(2S,3Z)-3-pentenylsulfinyl]-benzene
Synonyms: 1-(RS_S)-[5-N-methylcarbonyloxy-2-methyl-(2S,3Z)-3-pentenylsulfinyl]-benzene
CAS NO:689283-27-0
Molecular Formula:
Molecular Weight: 281.376
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: 1-(RS_S)-[5-N-methylcarbonyloxy-2-methyl-(2S,3Z)-3-pentenylsulfinyl]-benzene(CAS DataBase Reference)
NIST Chemistry Reference: 1-(RS_S)-[5-N-methylcarbonyloxy-2-methyl-(2S,3Z)-3-pentenylsulfinyl]-benzene(689283-27-0)
EPA Substance Registry System: 1-(RS_S)-[5-N-methylcarbonyloxy-2-methyl-(2S,3Z)-3-pentenylsulfinyl]-benzene(689283-27-0)

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: 689283-27-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 689283-27-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,9,2,8 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 689283-27:
(8*6)+(7*8)+(6*9)+(5*2)+(4*8)+(3*3)+(2*2)+(1*7)=220
220 % 10 = 0
So 689283-27-0 is a valid CAS Registry Number.

689283-27-0Upstream product

689283-27-0Downstream Products

689283-28-1 2-bromo-1-N-methylcarbonyloxy-4-methyl-5(RS_S)-phenylsulfinyl-(2R,3R,4S)-pentan-3-ol

689283-27-0Relevant academic research and scientific papers

Modular and stereoselective formal synthesis of MeBmt, an unusual amino acid constituent of cyclosporin A

Raghavan, Sadagopan,Rasheed, M. Abdul

, p. 3059 - 3065 (2004)

A convergent, flexible and stereoselective formal synthesis of MeBmt, the nonproteinogenic amino acid constituent of cyclosporin A is disclosed. The sulfinyl moiety has been exploited as the internal nucleophile to stereo- and regioselectively functionalize an allylic carbamate.

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