Cas 1007123-31-0,((S)-2,2-dimethyl-1-oxo-1-((S)-2-oxoazepan-3-ylamino)decan-3-yl) (2S)-2-(benzyloxycarbonylamino)-6-(N-(benzyloxy)formamido)hexanoate

1007123-31-0

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Basic information

Product Name: ((S)-2,2-dimethyl-1-oxo-1-((S)-2-oxoazepan-3-ylamino)decan-3-yl) (2S)-2-(benzyloxycarbonylamino)-6-(N-(benzyloxy)formamido)hexanoate
Synonyms: ((S)-2,2-dimethyl-1-oxo-1-((S)-2-oxoazepan-3-ylamino)decan-3-yl) (2S)-2-(benzyloxycarbonylamino)-6-(N-(benzyloxy)formamido)hexanoate
CAS NO:1007123-31-0
Molecular Formula:
Molecular Weight: 722.923
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: ((S)-2,2-dimethyl-1-oxo-1-((S)-2-oxoazepan-3-ylamino)decan-3-yl) (2S)-2-(benzyloxycarbonylamino)-6-(N-(benzyloxy)formamido)hexanoate(CAS DataBase Reference)
NIST Chemistry Reference: ((S)-2,2-dimethyl-1-oxo-1-((S)-2-oxoazepan-3-ylamino)decan-3-yl) (2S)-2-(benzyloxycarbonylamino)-6-(N-(benzyloxy)formamido)hexanoate(1007123-31-0)
EPA Substance Registry System: ((S)-2,2-dimethyl-1-oxo-1-((S)-2-oxoazepan-3-ylamino)decan-3-yl) (2S)-2-(benzyloxycarbonylamino)-6-(N-(benzyloxy)formamido)hexanoate(1007123-31-0)

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: 1007123-31-0(Hazardous Substances Data)

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1007123-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1007123-31-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,1,2 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1007123-31:
(9*1)+(8*0)+(7*0)+(6*7)+(5*1)+(4*2)+(3*3)+(2*3)+(1*1)=80
80 % 10 = 0
So 1007123-31-0 is a valid CAS Registry Number.

1007123-31-0Upstream product

1007123-31-0Downstream Products

1007123-32-1 C₃₂H₅₂N₄O₆

1007123-31-0Relevant academic research and scientific papers

Syntheses and biological activity of amamistatin B and analogs

Fennell, Kelley A.,Moellmann, Ute,Miller, Marvin J.

, p. 1018 - 1024 (2008)

(Chemical Equation Presented) Amamistatins A and B, natural products isolated from a strain of Nocardia, showed growth inhibition against three human tumor cell lines (IC50 0.24-0.56 μM). Structurally related mycobactins affect the growth of bo

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