Cas 1246212-47-4,(2R,3R)-2-(benzyloxy)-1-[(S)-4-benzyl-2-thioxooxazolidin-3-yl]-3-hydroxyhexan-1-one

1246212-47-4

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Basic information

Product Name: (2R,3R)-2-(benzyloxy)-1-[(S)-4-benzyl-2-thioxooxazolidin-3-yl]-3-hydroxyhexan-1-one
Synonyms: (2R,3R)-2-(benzyloxy)-1-[(S)-4-benzyl-2-thioxooxazolidin-3-yl]-3-hydroxyhexan-1-one
CAS NO:1246212-47-4
Molecular Formula:
Molecular Weight: 413.538
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: (2R,3R)-2-(benzyloxy)-1-[(S)-4-benzyl-2-thioxooxazolidin-3-yl]-3-hydroxyhexan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R)-2-(benzyloxy)-1-[(S)-4-benzyl-2-thioxooxazolidin-3-yl]-3-hydroxyhexan-1-one(1246212-47-4)
EPA Substance Registry System: (2R,3R)-2-(benzyloxy)-1-[(S)-4-benzyl-2-thioxooxazolidin-3-yl]-3-hydroxyhexan-1-one(1246212-47-4)

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: 1246212-47-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1246212-47-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,2,1 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1246212-47:
(9*1)+(8*2)+(7*4)+(6*6)+(5*2)+(4*1)+(3*2)+(2*4)+(1*7)=124
124 % 10 = 4
So 1246212-47-4 is a valid CAS Registry Number.

1246212-47-4Upstream product

1246212-47-4Downstream Products

1246212-46-3 (2R,3R)-2-(benzyloxy)-1-[(S)-4-benzyl-2-thioxooxazolidin-3-yl]-3-(tert-butyldimethylsilyloxy)hexan-1-one

1246212-47-4Relevant academic research and scientific papers

A stereoselective aldol approach for the total synthesis of herbarumin I and stagonolide A

Srihari,Rao, G. Maheswara,Rao, R. Srinivasa,Yadav

experimental part, p. 2407 - 2412 (2010/09/04)

A stereoselective total synthesis of phytotoxic compounds herbarumin I and stagonolide A has been achieved utilizing Crimmins protocol for non-Evans anti-aldol approach and a ring-closing olefin metathesis reaction as the key steps. Georg Thieme Verlag St

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