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5434-21-9

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5434-21-9 Usage

Chemical Properties

Beige powder

Check Digit Verification of cas no

The CAS Registry Mumber 5434-21-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5434-21:
(6*5)+(5*4)+(4*3)+(3*4)+(2*2)+(1*1)=79
79 % 10 = 9
So 5434-21-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO4/c9-4-1-2-5(7(10)11)6(3-4)8(12)13/h1-3H,9H2,(H,10,11)(H,12,13)/p-2

5434-21-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Alfa Aesar

  • (L03333)  4-Aminophthalic acid, 98%   

  • 5434-21-9

  • 1g

  • 544.0CNY

  • Detail
  • Alfa Aesar

  • (L03333)  4-Aminophthalic acid, 98%   

  • 5434-21-9

  • 5g

  • 1844.0CNY

  • Detail
  • Aldrich

  • (524716)  4-Aminophthalicacid  97%

  • 5434-21-9

  • 524716-1G

  • 374.40CNY

  • Detail
  • Aldrich

  • (524716)  4-Aminophthalicacid  97%

  • 5434-21-9

  • 524716-10G

  • 2,230.02CNY

  • Detail

5434-21-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Aminophthalic acid

1.2 Other means of identification

Product number -
Other names 4-Amino-1,2-benzenedicarboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5434-21-9 SDS

5434-21-9Downstream Products

5434-21-9Relevant articles and documents

Metal organic framework material loaded with tetrakis-(N-methylallylamine)phthalocyanine compound, and preparation method and application thereof

-

Paragraph 0074-0076, (2019/11/20)

The invention relates to the technical field of preparation of phthalocyanine compounds, in particular to a metal organic framework material loaded with a tetrakis-(N-methylallylamine)phthalocyanine compound, and a preparation method and application thereof. The metal organic framework material loaded with the tetrakis-(N-methylallylamine)phthalocyanine compound is composed of the tetrakis-(N-methylallylamine)phthalocyanine compound and a ZIF-series metal organic framework material, wherein the tetrakis-(N-methylallylamine)phthalocyanine compound is encapsulated in the ZIF-series metal organicframework material. The metal organic framework material loaded with a tetrakis-(N-methylallylamine)phthalocyanine compound of the invention effectively overcomes the problem that phthalocyanine molecular aggregate, as an anti-cancer photosensitizer or a photothermal conversion agent, does not dissolve or disperse in an aqueous phase system in the prior art, successfully realizes red shifting ofan absorption peak to a near-infrared region (700 nm), solves the problem that phthalocyanine molecules cannot be used for deep tumor treatment in the prior art, and is beneficial for deep treatment of tumors.

Diels-Alder reaction of ethyl 3-benzamido-2-oxo-6-(trifluoromethyl)-2H- pyran-5-carboxylate with alkoxyalkenes as an effective approach to trifluoromethyl-containing 3-aminobenzoic acid derivatives

Kondratov, Ivan S.,Tolmachova, Nataliya A.,Dolovanyuk, Violetta G.,Gerus, Igor I.,Bergander, Klaus,Daniliuc, Constantin-Gabriel,Haufe, Guenter

supporting information, p. 2443 - 2450 (2014/05/06)

The Diels-Alder reactions of ethyl 3-benzamido-2-oxo-6-(trifluoromethyl)- 2H-pyran-5-carboxylate with ethyl vinyl ether, 2-methoxypropene, and 1-ethoxypropene were investigated. Under different reaction conditions, intermediate oxabicyclo[2.2.2]octenones,

Vitamin D analogues

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Page column 20, (2010/02/05)

The invention concerns novel bi-aromatic compounds having the formula: which are analogs of vitamin D, the process of preparing them, as well as their use in pharmaceutical compositions in human or veterinary medicine, particularly in dermatology, cancer treatment, treatment of auto-immune diseases, and in organ or tissue transplants. Cosmetic compositions and methods of use are also included.

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