Cas 1316152-75-6,(2S,5R,6R)-1-benzyloxy-7-tert-butyldiphenylsilyloxy-5-hydroxy-2,6-dimethyl-3-heptanone

1316152-75-6

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Basic information

Product Name: (2S,5R,6R)-1-benzyloxy-7-tert-butyldiphenylsilyloxy-5-hydroxy-2,6-dimethyl-3-heptanone
Synonyms:
CAS NO:1316152-75-6
Molecular Formula:
Molecular Weight: 518.769
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: (2S,5R,6R)-1-benzyloxy-7-tert-butyldiphenylsilyloxy-5-hydroxy-2,6-dimethyl-3-heptanone(CAS DataBase Reference)
NIST Chemistry Reference: (2S,5R,6R)-1-benzyloxy-7-tert-butyldiphenylsilyloxy-5-hydroxy-2,6-dimethyl-3-heptanone(1316152-75-6)
EPA Substance Registry System: (2S,5R,6R)-1-benzyloxy-7-tert-butyldiphenylsilyloxy-5-hydroxy-2,6-dimethyl-3-heptanone(1316152-75-6)

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: 1316152-75-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1316152-75-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,6,1,5 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1316152-75:
(9*1)+(8*3)+(7*1)+(6*6)+(5*1)+(4*5)+(3*2)+(2*7)+(1*5)=126
126 % 10 = 6
So 1316152-75-6 is a valid CAS Registry Number.

1316152-75-6Upstream product

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1316152-75-6Relevant academic research and scientific papers

Highly stereoselective titanium-mediated aldol reaction from (S)-4-benzyloxy-3-methyl-2-butanone

Zambrana, Joana,Romea, Pedro,Urpi, Felix,Lujan, Cristina

experimental part, p. 8575 - 8587 (2012/01/03)

Substrate-controlled titanium-mediated aldol reactions from (S)-4-benzyloxy-3-methyl-2-butanone provide satisfactory levels of 2,5-syn asymmetric induction if they are carried out in the presence of a second equivalent of TiCl4. Such reactions

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