Cas 134860-60-9,(S)-2-((1R,2R,3R)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-6-hydroxy-5,6-dimethyl-6H-pyran-3-one

134860-60-9

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Basic information

Product Name: (S)-2-((1R,2R,3R)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-6-hydroxy-5,6-dimethyl-6H-pyran-3-one
Synonyms: (S)-2-((1R,2R,3R)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-6-hydroxy-5,6-dimethyl-6H-pyran-3-one
CAS NO:134860-60-9
Molecular Formula:
Molecular Weight: 348.439
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: (S)-2-((1R,2R,3R)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-6-hydroxy-5,6-dimethyl-6H-pyran-3-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-((1R,2R,3R)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-6-hydroxy-5,6-dimethyl-6H-pyran-3-one(134860-60-9)
EPA Substance Registry System: (S)-2-((1R,2R,3R)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-6-hydroxy-5,6-dimethyl-6H-pyran-3-one(134860-60-9)

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: 134860-60-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134860-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,6 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 134860-60:
(8*1)+(7*3)+(6*4)+(5*8)+(4*6)+(3*0)+(2*6)+(1*0)=129
129 % 10 = 9
So 134860-60-9 is a valid CAS Registry Number.

134860-60-9Upstream product

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134860-60-9Relevant academic research and scientific papers

ASYMMETRIC ALDOL REACTIONS USING CHIRAL BORON REAGENTS: APPLICATION TO THE SYNTHESIS OF TIRANDAMYCIN A

Paterson, Ian,Lister, M. Anne,Ryan, Glen R.

, p. 1749 - 1752 (2007/10/02)

The bicyclic acetal 1, a key intermediate in previous synthetic studies on tirandamycin A, has been prepared in enantiomerically pure form starting from the (R)-ethylketone 2 and the aldehyde 3.A reagent controlled aldol reaction using (-)-(Ipc)2BOTf sele

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