Cas 81102-18-3,Acetic acid (2S,3R,4S,5S)-3-acetoxy-2-benzyloxy-5-((R)-2-benzyloxycarbonylamino-propionylamino)-tetrahydro-pyran-4-yl ester

81102-18-3

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Basic information

Product Name: Acetic acid (2S,3R,4S,5S)-3-acetoxy-2-benzyloxy-5-((R)-2-benzyloxycarbonylamino-propionylamino)-tetrahydro-pyran-4-yl ester
Synonyms:
CAS NO:81102-18-3
Molecular Formula:
Molecular Weight: 528.559
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: Acetic acid (2S,3R,4S,5S)-3-acetoxy-2-benzyloxy-5-((R)-2-benzyloxycarbonylamino-propionylamino)-tetrahydro-pyran-4-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2S,3R,4S,5S)-3-acetoxy-2-benzyloxy-5-((R)-2-benzyloxycarbonylamino-propionylamino)-tetrahydro-pyran-4-yl ester(81102-18-3)
EPA Substance Registry System: Acetic acid (2S,3R,4S,5S)-3-acetoxy-2-benzyloxy-5-((R)-2-benzyloxycarbonylamino-propionylamino)-tetrahydro-pyran-4-yl ester(81102-18-3)

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: 81102-18-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 81102-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,0 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81102-18:
(7*8)+(6*1)+(5*1)+(4*0)+(3*2)+(2*1)+(1*8)=83
83 % 10 = 3
So 81102-18-3 is a valid CAS Registry Number.

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81102-18-3Relevant academic research and scientific papers

SYNTHESIS AND BIOLOGICAL ACTIVITES OF 4-(D-ALANYLAMINO)-2-AMINO-2,3,4-TRIDEOXY-L-THREO-PENTOSE (3-DEOXYPRUMYCIN)

Hashimoto, Hironobu,Koichi, Araki,Miazawa, Ken-Ichi,Yoshimura, Juji

, p. 59 - 69 (1982)

Three analogs of prumycin , i.e., the 3-deoxygenated (1), that having the 2-amino and 3-hydroxyl groups interchanged (2), and that having C-2 deaminated (3), were synthesized.Examination of the antifunga

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