Cas 260783-49-1,5-[3-(4,4-diethoxy-butyl)-thioureido]-2-(6-hydroxy-3-oxo-3<i>H</i>-xanthen-9-yl)-benzoic acid

260783-49-1

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Basic information

Product Name: 5-[3-(4,4-diethoxy-butyl)-thioureido]-2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-benzoic acid
Synonyms: 5-[3-(4,4-diethoxy-butyl)-thioureido]-2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-benzoic acid
CAS NO:260783-49-1
Molecular Formula:
Molecular Weight: 550.632
EINECS: N/A
Product Categories: N/A
Mol File: 260783-49-1.mol
Article Data: 1

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: 5-[3-(4,4-diethoxy-butyl)-thioureido]-2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-benzoic acid(CAS DataBase Reference)
NIST Chemistry Reference: 5-[3-(4,4-diethoxy-butyl)-thioureido]-2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-benzoic acid(260783-49-1)
EPA Substance Registry System: 5-[3-(4,4-diethoxy-butyl)-thioureido]-2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-benzoic acid(260783-49-1)

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: 260783-49-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 260783-49-1 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, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 260783-49:
(8*2)+(7*6)+(6*0)+(5*7)+(4*8)+(3*3)+(2*4)+(1*9)=151
151 % 10 = 1
So 260783-49-1 is a valid CAS Registry Number.

260783-49-1Upstream product

260783-49-1Downstream Products

260783-49-1Relevant articles and documents

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 (2007/10/03)

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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