Cas 348584-45-2,(2R,3R)-2-(tert-Butyldimethylsiloxy)-1,4-bis[(4-methylphenyl)sulfonyloxy]-3-[(4-methylphenyl)sulfonylamino]butane

348584-45-2

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Basic information

Product Name: (2R,3R)-2-(tert-Butyldimethylsiloxy)-1,4-bis[(4-methylphenyl)sulfonyloxy]-3-[(4-methylphenyl)sulfonylamino]butane
Synonyms: (2R,3R)-2-(tert-Butyldimethylsiloxy)-1,4-bis[(4-methylphenyl)sulfonyloxy]-3-[(4-methylphenyl)sulfonylamino]butane
CAS NO:348584-45-2
Molecular Formula:
Molecular Weight: 697.967
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-(tert-Butyldimethylsiloxy)-1,4-bis[(4-methylphenyl)sulfonyloxy]-3-[(4-methylphenyl)sulfonylamino]butane(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R)-2-(tert-Butyldimethylsiloxy)-1,4-bis[(4-methylphenyl)sulfonyloxy]-3-[(4-methylphenyl)sulfonylamino]butane(348584-45-2)
EPA Substance Registry System: (2R,3R)-2-(tert-Butyldimethylsiloxy)-1,4-bis[(4-methylphenyl)sulfonyloxy]-3-[(4-methylphenyl)sulfonylamino]butane(348584-45-2)

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: 348584-45-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 348584-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,8,5,8 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 348584-45:
(8*3)+(7*4)+(6*8)+(5*5)+(4*8)+(3*4)+(2*4)+(1*5)=182
182 % 10 = 2
So 348584-45-2 is a valid CAS Registry Number.

348584-45-2Upstream product

348584-45-2Downstream Products

348584-48-5 (2R)-1-[(4-Methylphenyl)sulfonyl]-2-[(2R)-oxiran-2-yl]aziridine

348584-45-2Relevant academic research and scientific papers

1,2-epimino-3,4-epoxybutane: A versatile chiral building block

Harms,Schaumann,Adiwidjaja

, p. 577 - 580 (2007/10/03)

The synthesis of enantiomerically pure 1,2-epimino-3,4-epoxy-(N-toluenesulfonyl)butane (6) in the S,R-(erythro) and R,R-(threo) configurations is described. This building block offers a new route to targets with an 1,2-aminohydroxy functionality. As an example, the new 1,4-biselectrophile is employed in a cyclopentane synthesis.

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