Cas 1300637-98-2,(3S,6S,7R)-3-(benzyloxymethyl)-7-(hydroxymethyl)-6-hydroxy-4-N-methyl-1,4-diazepan-2-one

1300637-98-2

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Basic information

Product Name: (3S,6S,7R)-3-(benzyloxymethyl)-7-(hydroxymethyl)-6-hydroxy-4-N-methyl-1,4-diazepan-2-one
Synonyms: (3S,6S,7R)-3-(benzyloxymethyl)-7-(hydroxymethyl)-6-hydroxy-4-N-methyl-1,4-diazepan-2-one
CAS NO:1300637-98-2
Molecular Formula:
Molecular Weight: 294.351
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: (3S,6S,7R)-3-(benzyloxymethyl)-7-(hydroxymethyl)-6-hydroxy-4-N-methyl-1,4-diazepan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3S,6S,7R)-3-(benzyloxymethyl)-7-(hydroxymethyl)-6-hydroxy-4-N-methyl-1,4-diazepan-2-one(1300637-98-2)
EPA Substance Registry System: (3S,6S,7R)-3-(benzyloxymethyl)-7-(hydroxymethyl)-6-hydroxy-4-N-methyl-1,4-diazepan-2-one(1300637-98-2)

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: 1300637-98-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1300637-98-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,0,6,3 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1300637-98:
(9*1)+(8*3)+(7*0)+(6*0)+(5*6)+(4*3)+(3*7)+(2*9)+(1*8)=122
122 % 10 = 2
So 1300637-98-2 is a valid CAS Registry Number.

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1300637-98-2Relevant academic research and scientific papers

Synthesis and biological evaluation of a diazepanone-based library of liposidomycins analogs as MraY inhibitors

Mravljak, Janez,Monasson, Olivier,Al-Dabbagh, Bayan,Crouvoisier, Muriel,Bouhss, Ahmed,Gravier-Pelletier, Christine,Merrer, Yves Le

, p. 1582 - 1592 (2011)

New inhibitors of the bacterial tranferase MraY are described. A scaffold strategy based on the diazepanone central core of liposidomycins, natural inhibitors of MraY has been developed. It involves the introduction of key structural fragments required fo

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