Cas 260783-50-4,2-(6-hydroxy-3-oxo-3<i>H</i>-xanthen-9-yl)-5-[3-(4-oxo-butyl)-thioureido]-benzoic acid

260783-50-4

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Basic information

Product Name: 2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-5-[3-(4-oxo-butyl)-thioureido]-benzoic acid
Synonyms: 2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-5-[3-(4-oxo-butyl)-thioureido]-benzoic acid
CAS NO:260783-50-4
Molecular Formula:
Molecular Weight: 476.51
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: 2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-5-[3-(4-oxo-butyl)-thioureido]-benzoic acid(CAS DataBase Reference)
NIST Chemistry Reference: 2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-5-[3-(4-oxo-butyl)-thioureido]-benzoic acid(260783-50-4)
EPA Substance Registry System: 2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-5-[3-(4-oxo-butyl)-thioureido]-benzoic acid(260783-50-4)

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: 260783-50-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 260783-50-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,0,7,8 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 260783-50:
(8*2)+(7*6)+(6*0)+(5*7)+(4*8)+(3*3)+(2*5)+(1*0)=144
144 % 10 = 4
So 260783-50-4 is a valid CAS Registry Number.

260783-50-4Upstream product

1173-43-9 fluoresceinyl 5-isothiocyanate

260783-50-4Downstream Products

260783-50-4Relevant academic research and scientific papers

Synthesis of nucleoside triphosphates that contain an aminooxy function for 'post-amplification labelling'

Trevisiol, Emmanuelle,Defrancq, Eric,Lhomme, Jean,Laayoun, Ali,Cros, Philippe

, p. 211 - 217 (2000)

Preparation of the uridine and adenosine triphosphates 1 and 2 bearing a linker with a terminal aminooxy group is described. Both 1 and 2 react readily with the aldehydic fluorescein derivative 15. They could each be incorporated into a 330-mer fragment w

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