Cas 1224587-91-0,(4R,5R)-4-benzoyl-5-(tert-butyldimethylsilyloxy)methyl-2,2-dimethyl-1,3-dioxolane

1224587-91-0

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Basic information

Product Name: (4R,5R)-4-benzoyl-5-(tert-butyldimethylsilyloxy)methyl-2,2-dimethyl-1,3-dioxolane
Synonyms: (4R,5R)-4-benzoyl-5-(tert-butyldimethylsilyloxy)methyl-2,2-dimethyl-1,3-dioxolane
CAS NO:1224587-91-0
Molecular Formula:
Molecular Weight: 350.53
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: (4R,5R)-4-benzoyl-5-(tert-butyldimethylsilyloxy)methyl-2,2-dimethyl-1,3-dioxolane(CAS DataBase Reference)
NIST Chemistry Reference: (4R,5R)-4-benzoyl-5-(tert-butyldimethylsilyloxy)methyl-2,2-dimethyl-1,3-dioxolane(1224587-91-0)
EPA Substance Registry System: (4R,5R)-4-benzoyl-5-(tert-butyldimethylsilyloxy)methyl-2,2-dimethyl-1,3-dioxolane(1224587-91-0)

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: 1224587-91-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1224587-91-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,5,8 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1224587-91:
(9*1)+(8*2)+(7*2)+(6*4)+(5*5)+(4*8)+(3*7)+(2*9)+(1*1)=160
160 % 10 = 0
So 1224587-91-0 is a valid CAS Registry Number.

1224587-91-0Upstream product

1224587-91-0Downstream Products

1224587-93-2 (4S,5R)-5-(tert-butyldimethylsilyloxy)methyl-2,2-dimethyl-4-(1-phenyl(hydroxy)methyl)-1,3-dioxolane

1224587-91-0Relevant academic research and scientific papers

Aspects of stereocontrol in the L-Selectride reduction of 4-acyl-1,3-dioxolane derivatives

Robertson, Jeremy,Unsworth, William P.,Lamont, Scott G.

, p. 2363 - 2372 (2010)

The application of L-Selectride, either alone or in combination with ZnCl2, to aryl ketones 1, 8 and 11 resulted in highly anti-stereoselective reduction. In contrast, lactols 22 and 23 gave a moderate syn-preference using L-Selectride alone an

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