Cas 882316-92-9,N-(4-hydroxy-9,10-dioxo-2-phenoxy-9,10-dihydroanthracen-1-yl)benzamide

882316-92-9

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Basic information

Product Name: N-(4-hydroxy-9,10-dioxo-2-phenoxy-9,10-dihydroanthracen-1-yl)benzamide
Synonyms: N-(4-hydroxy-9,10-dioxo-2-phenoxy-9,10-dihydroanthracen-1-yl)benzamide
CAS NO:882316-92-9
Molecular Formula:
Molecular Weight: 435.436
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: N-(4-hydroxy-9,10-dioxo-2-phenoxy-9,10-dihydroanthracen-1-yl)benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(4-hydroxy-9,10-dioxo-2-phenoxy-9,10-dihydroanthracen-1-yl)benzamide(882316-92-9)
EPA Substance Registry System: N-(4-hydroxy-9,10-dioxo-2-phenoxy-9,10-dihydroanthracen-1-yl)benzamide(882316-92-9)

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: 882316-92-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 882316-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,3,1 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 882316-92:
(8*8)+(7*8)+(6*2)+(5*3)+(4*1)+(3*6)+(2*9)+(1*2)=189
189 % 10 = 9
So 882316-92-9 is a valid CAS Registry Number.

882316-92-9Upstream product

882316-92-9Downstream Products

1160362-67-3 N-(4-hydroxy-9,10-dioxo-2-piperidino-9,10-dihydroanthracen-1-yl)benzamide

882316-92-9Relevant academic research and scientific papers

DYE AND DYEING METHOD

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Paragraph 0030, (2017/11/03)

A dyeing method is provided, which includes dyeing a dye to a fiber by a supercritical fluid, wherein the dye has a chemical structure of: . R1 is -A-Ph-(R)1-3. R2 is H or -OPh. R3 is -A-Ph-(R)1-3, H, -NH2

Synthesis of water-soluble large naturalised dyes through double glycoconjugation

Isaad, Jalal,Rolla, Massimo,Bianchini, Roberto

experimental part, p. 2748 - 2764 (2009/08/16)

Recently we started to develop a new class of dyes based upon the glycoconjugation of disperse dyes with mono- or disaccharides. We used the term "naturalised" to describe these dyes because we used natural lactose in the glycoconjugation process, and also because they are similar to real natural dyes, the hydrosolubility of which is based upon the saccharidic moiety attached to the chromophore, as in carminic acid or carthamin. Synthetic dyes submitted to the process of naturalisation consist of small chromophoric molecules, prevalently azoic, whereas larger dye molecules with a higher mass did not show appreciable solubility in water when a single molecule of lactose was added through a bivalent spacer, which is in contrast to the smaller dyes. To overcome this difficulty, herein we present the first approach to the insertion of two lactose units by a double glycoconjugation process. The procedure here presented allows the successful insertion of a spacer, the malonic acid, which can be linked with two lactose units so that even large dyes become soluble. Wiley-VCH Verlag GmbH & Co. KGaA.

Reactions of 1-acylamino- and 1-methylsulfonylamino-2-aryloxy-4-hydroxy-9, 10-anthraquinones with secondary amines

Beresnev,Sokolova,Gritsan,Gornostaev

experimental part, p. 1490 - 1493 (2009/06/21)

Reactions of 1-acylamino-4-hydroxy-2-phenoxy-9,10-anthraquinones with piperidine resulted in replacement of the phenoxy group by piperidino, while 1-methylsulfonyl-2-aryloxy-4-hydroxy-9,10-anthraquinones reacted with secondary amines to give products of n

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