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5-(acetylamino)-2-furoic acid is a chemical compound with the molecular formula C7H7NO4. It is a derivative of 2-furoic acid, where an acetylamino group (-NHCOCH3) is attached to the 5-position of the furan ring. This organic compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain antibiotics and other bioactive molecules. Its structure features a furan ring, which is a five-membered ring containing four carbon atoms and one oxygen atom, and an acetylamino group that provides additional functional groups for further chemical reactions. The compound's properties, such as its reactivity and solubility, make it a valuable building block in the development of new drugs and chemical products.

772-69-0

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772-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 772-69-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 772-69:
(5*7)+(4*7)+(3*2)+(2*6)+(1*9)=90
90 % 10 = 0
So 772-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO4/c1-4(9)8-6-3-2-5(12-6)7(10)11/h2-3H,1H3,(H,8,9)(H,10,11)/p-1

772-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-acetamidofuran-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-Acetamino-brenzschleimsaeure

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:772-69-0 SDS

772-69-0Downstream Products

772-69-0Relevant academic research and scientific papers

Diarylamide compound and application thereof

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Paragraph 0317-0319; 0322, (2020/12/31)

The invention discloses a use of a diarylamide compound with a structure shown as a formula (I), and a pharmaceutically acceptable salt thereof in the preparation of a medicine serving as a urea transporter inhibitor, and the novel diarylamide compound. T

REDUCTIVE ACETYLATION OF NITROCARBOXYLIC ACIDS OF THE THIOPHENE AND FURAN SERIES OR THEIR ESTERS

Gol'dfarb, Ya. L.,Bulgakova, V. N.,Fabrichnyi, B. P.

, p. 1283 - 1286 (2007/10/02)

The corresponding 4-acetylamino-2-thiophenecarboxylic acids or their esters were produced by the action of reduced iron on solutions of 4-nitro-2-thiophenecarboxylic acid, its derivatives, or their esters in a mixture of acetic acid and acetic anhydride.Esters of 5-acetylamino-2-thiophenecarboxylic or 5-acetylamino-2-furancarboxylic acids are formed from esters of 5-nitro-2-thiophenecarboxylic or 5-nitro-2-furancarboxylic acids.Free 5-nitro-2-thiophenecarboxylic and 5-nitro-2-furancarboxylic acids are entirely decomposed under the conditions of reductive acetylation by iron.The ester of 5-acetylamino-3-thiphenecarboxylic acid was obtained from methyl ester of 5-nitro-3-thiophenecarboxylic acid.

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