Cas 39484-05-4,2-methyl-3-(N-acetylcystein-S-yl)-1,4-naphthoquinone

39484-05-4

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Basic information

Product Name: 2-methyl-3-(N-acetylcystein-S-yl)-1,4-naphthoquinone
Synonyms: 2-methyl-3-(N-acetylcystein-S-yl)-1,4-naphthoquinone
CAS NO:39484-05-4
Molecular Formula: C16H15 N O5 S
Molecular Weight: 333.36
EINECS: N/A
Product Categories: N/A
Mol File: 39484-05-4.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 615.4°Cat760mmHg
Flash Point: 326°C
Appearance: /
Density: 1.41g/cm³
Vapor Pressure: 5.31E-16mmHg at 25°C
Refractive Index: 1.633
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-methyl-3-(N-acetylcystein-S-yl)-1,4-naphthoquinone(CAS DataBase Reference)
NIST Chemistry Reference: 2-methyl-3-(N-acetylcystein-S-yl)-1,4-naphthoquinone(39484-05-4)
EPA Substance Registry System: 2-methyl-3-(N-acetylcystein-S-yl)-1,4-naphthoquinone(39484-05-4)

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: 39484-05-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 39484-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,4,8 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 39484-05:
(7*3)+(6*9)+(5*4)+(4*8)+(3*4)+(2*0)+(1*5)=144
144 % 10 = 4
So 39484-05-4 is a valid CAS Registry Number.

InChI:InChI=1/C16H15NO5S/c1-8-13(19)10-5-3-4-6-11(10)14(20)15(8)23-7-12(16(21)22)17-9(2)18/h3-6,12H,7H2,1-2H3,(H,17,18)(H,21,22)/t12-/m0/s1

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39484-05-4Relevant academic research and scientific papers

Site-specific binding of quinones to proteins through thiol addition and addition-elimination reactions

Li, Wen-Wu,Heinze, Juergen,Haehnel, Wolfgang

, p. 6140 - 6141 (2005)

Ubiquinone-0, menaquinone-0, and 2,3,5-trimethyl-1,4-benzoquinone were site-specifically bound to free cysteine of proteins (yeast iso-1 cytochrome c as a model protein) through thioether bond formation. Model thioether quinone conjugates showed unexpecte

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