Cas 112289-33-5,5-acetamido-8-O-allyl-6-O-benzyl-5-deoxy-1,2-O-isopropylidene-3-O-methylthiomethyl-β-L-erythro-D-allooctofuranose-(1,4)

112289-33-5

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Basic information

Product Name: 5-acetamido-8-O-allyl-6-O-benzyl-5-deoxy-1,2-O-isopropylidene-3-O-methylthiomethyl-β-L-erythro-D-allooctofuranose-(1,4)
Synonyms: 5-acetamido-8-O-allyl-6-O-benzyl-5-deoxy-1,2-O-isopropylidene-3-O-methylthiomethyl-β-L-erythro-D-allooctofuranose-(1,4)
CAS NO:112289-33-5
Molecular Formula:
Molecular Weight: 511.637
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: 5-acetamido-8-O-allyl-6-O-benzyl-5-deoxy-1,2-O-isopropylidene-3-O-methylthiomethyl-β-L-erythro-D-allooctofuranose-(1,4)(CAS DataBase Reference)
NIST Chemistry Reference: 5-acetamido-8-O-allyl-6-O-benzyl-5-deoxy-1,2-O-isopropylidene-3-O-methylthiomethyl-β-L-erythro-D-allooctofuranose-(1,4)(112289-33-5)
EPA Substance Registry System: 5-acetamido-8-O-allyl-6-O-benzyl-5-deoxy-1,2-O-isopropylidene-3-O-methylthiomethyl-β-L-erythro-D-allooctofuranose-(1,4)(112289-33-5)

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: 112289-33-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112289-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,8 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 112289-33:
(8*1)+(7*1)+(6*2)+(5*2)+(4*8)+(3*9)+(2*3)+(1*3)=105
105 % 10 = 5
So 112289-33-5 is a valid CAS Registry Number.

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112289-33-5Relevant academic research and scientific papers

Synthetic Approach toward Antibiotic Ezomycins. III. Synthesis of a Protected Derivative of the Octose Moiety

Sakanaka, Osamu,Ohmori, Takashi,Kozaki, Shuji,Suami, Tetsuo

, p. 1057 - 1062 (1987)

A protected derivative of the octose moiety of antibiotic ezomycins A1 and A2, 4-N-benzoyl-1--cytosine, has been synthe

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