Cas 112138-78-0,ethyl 4(R)-<(1R)-4(R)-<(benzyloxy)methyl>-4-hydroxy-3(R),8(S)-dimethyl-2,9-dioxabicyclo<3.3.1>non-5(Z)-en-1-yl>-2-methylpent-2(E)-enoate

112138-78-0

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Basic information

Product Name: ethyl 4(R)-<(1R)-4(R)-<(benzyloxy)methyl>-4-hydroxy-3(R),8(S)-dimethyl-2,9-dioxabicyclo<3.3.1>non-5(Z)-en-1-yl>-2-methylpent-2(E)-enoate
Synonyms: ethyl 4(R)-<(1R)-4(R)-<(benzyloxy)methyl>-4-hydroxy-3(R),8(S)-dimethyl-2,9-dioxabicyclo<3.3.1>non-5(Z)-en-1-yl>-2-methylpent-2(E)-enoate
CAS NO:112138-78-0
Molecular Formula:
Molecular Weight: 430.541
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: ethyl 4(R)-<(1R)-4(R)-<(benzyloxy)methyl>-4-hydroxy-3(R),8(S)-dimethyl-2,9-dioxabicyclo<3.3.1>non-5(Z)-en-1-yl>-2-methylpent-2(E)-enoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 4(R)-<(1R)-4(R)-<(benzyloxy)methyl>-4-hydroxy-3(R),8(S)-dimethyl-2,9-dioxabicyclo<3.3.1>non-5(Z)-en-1-yl>-2-methylpent-2(E)-enoate(112138-78-0)
EPA Substance Registry System: ethyl 4(R)-<(1R)-4(R)-<(benzyloxy)methyl>-4-hydroxy-3(R),8(S)-dimethyl-2,9-dioxabicyclo<3.3.1>non-5(Z)-en-1-yl>-2-methylpent-2(E)-enoate(112138-78-0)

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: 112138-78-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112138-78-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,3 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112138-78:
(8*1)+(7*1)+(6*2)+(5*1)+(4*3)+(3*8)+(2*7)+(1*8)=90
90 % 10 = 0
So 112138-78-0 is a valid CAS Registry Number.

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112138-78-0Relevant academic research and scientific papers

3-Acyltetramic acid antibiotics. 2. Synthesis of (+)-streptolic acid

Ireland,Smith

, p. 854 - 860 (1988)

An efficient synthesis of streptolic acid, a product obtained from cleavage of the antibiotic streptolydigin, is described. The approach is based on the use of D-( plus )-glucose for the source of absolute stereochemistry, and the transfer of asymmetry is

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