Cas 128286-15-7,3-((3aR,5S,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-3-hydroxy-butyric acid ethyl ester

128286-15-7

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Basic information

Product Name: 3-((3aR,5S,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-3-hydroxy-butyric acid ethyl ester
Synonyms:
CAS NO:128286-15-7
Molecular Formula:
Molecular Weight: 380.438
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: 3-((3aR,5S,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-3-hydroxy-butyric acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-((3aR,5S,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-3-hydroxy-butyric acid ethyl ester(128286-15-7)
EPA Substance Registry System: 3-((3aR,5S,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-3-hydroxy-butyric acid ethyl ester(128286-15-7)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 128286-15-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 128286-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,2,8 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 128286-15:
(8*1)+(7*2)+(6*8)+(5*2)+(4*8)+(3*6)+(2*1)+(1*5)=137
137 % 10 = 7
So 128286-15-7 is a valid CAS Registry Number.

128286-15-7Upstream product

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128286-15-7Relevant academic research and scientific papers

HIGHLY STEREOSELECTIVE APPROACH FOR β-HYDROXY-α-AMINO ACIDS FROM D-GLUCOSE : THE SYNTHESIS OF MeBmt

Rao, A.V. Rama,Yadav, J.S.,Chandrasekhar, S.,Rao, C. Srinivas

, p. 6769 - 6772 (2007/10/02)

A highly stereoselective protocol for the synthesis of β-hydroxy-α-amino acids from glucofuranose has been developed which has culminated in stereospecific synthesis of MeBmt - an unusual aminoacid component of immunosuppressive peptide cyclosporin.

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