Cas 554409-16-4,4-Thiazolecarboxylic acid, 2-[5-[[(1,1-dimethylethoxy)carbonyl]amino]-2-hydroxyphenyl]-4,5-dihydro -

554409-16-4

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Basic information

Product Name: 4-Thiazolecarboxylic acid, 2-[5-[[(1,1-dimethylethoxy)carbonyl]amino]-2-hydroxyphenyl]-4,5-dihydro -
Synonyms:
CAS NO:554409-16-4
Molecular Formula: C15H18N2O5S
Molecular Weight: 338.384
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: 4-Thiazolecarboxylic acid, 2-[5-[[(1,1-dimethylethoxy)carbonyl]amino]-2-hydroxyphenyl]-4,5-dihydro -(CAS DataBase Reference)
NIST Chemistry Reference: 4-Thiazolecarboxylic acid, 2-[5-[[(1,1-dimethylethoxy)carbonyl]amino]-2-hydroxyphenyl]-4,5-dihydro -(554409-16-4)
EPA Substance Registry System: 4-Thiazolecarboxylic acid, 2-[5-[[(1,1-dimethylethoxy)carbonyl]amino]-2-hydroxyphenyl]-4,5-dihydro -(554409-16-4)

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: 554409-16-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 554409-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,4,4,0 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 554409-16:
(8*5)+(7*5)+(6*4)+(5*4)+(4*0)+(3*9)+(2*1)+(1*6)=154
154 % 10 = 4
So 554409-16-4 is a valid CAS Registry Number.

554409-16-4Upstream product

554409-16-4Downstream Products

554409-17-5 t-butyl {4-hydroxy-3-[4'-(N-methoxy-N-methyl-carboxamido)-4',5'-dihydrothiazol-2'-yl]-phenyl}carbamate

554409-16-4Relevant academic research and scientific papers

Bacterial siderophores: Synthesis and biological activities of novel pyochelin analogues

Zamri,Schalk,Pattus,Abdallah

, p. 1147 - 1150 (2003)

The synthesis and biological activities of four pyochelin analogues substituted in different parts of the molecule are reported: 5-NHBoc-pyochelin, 3″N-Boc-pyochelin, 3″-nor-NH-pyochelin and neopyochelin II, the enantiomer of natural pyochelin. All these

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