Cas 136235-03-5,(E)-(2R,5S,6R)-7-Benzyloxy-6-methoxy-2,5-dimethyl-hept-3-enoic acid methyl ester

136235-03-5

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Basic information

Product Name: (E)-(2R,5S,6R)-7-Benzyloxy-6-methoxy-2,5-dimethyl-hept-3-enoic acid methyl ester
Synonyms: (E)-(2R,5S,6R)-7-Benzyloxy-6-methoxy-2,5-dimethyl-hept-3-enoic acid methyl ester
CAS NO:136235-03-5
Molecular Formula:
Molecular Weight: 306.402
EINECS: N/A
Product Categories: N/A
Mol File: 136235-03-5.mol
Article Data: 1

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: (E)-(2R,5S,6R)-7-Benzyloxy-6-methoxy-2,5-dimethyl-hept-3-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(2R,5S,6R)-7-Benzyloxy-6-methoxy-2,5-dimethyl-hept-3-enoic acid methyl ester(136235-03-5)
EPA Substance Registry System: (E)-(2R,5S,6R)-7-Benzyloxy-6-methoxy-2,5-dimethyl-hept-3-enoic acid methyl ester(136235-03-5)

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: 136235-03-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 136235-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,3 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 136235-03:
(8*1)+(7*3)+(6*6)+(5*2)+(4*3)+(3*5)+(2*0)+(1*3)=105
105 % 10 = 5
So 136235-03-5 is a valid CAS Registry Number.

136235-03-5Upstream product

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136235-03-5Relevant articles and documents

Remote Asymmetric Induction in Diastereoface Selective Addition Reactions of Optically Active α-Substituted-β-silyl (E)-Hexenoates with Achiral α-Alkoxy and β-Alkoxy Acetals

Panek, James S.,Yang, Michael

, p. 5755 - 5758 (2007/10/02)

Optically active and diastereomerically pure (E)-crotylsilanes 1 function as effective chiral carbon nucleophiles in trimethylsilyl trifluoromethanesulfonate (TMSOTf) catalyzed asymmetric addition reactions of achiral, α-alkoxy and β-alkoxy acetals 2, res

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