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54574-82-2

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  • China Largest factory Manufacturer Supply 2-[4-(Dibutylamino)-2-hydroxybenzoyl]benzoic acid CAS 54574-82-2

    Cas No: 54574-82-2

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54574-82-2 Usage

General Description

2-[4-(Dibutylamino)-2-hydroxybenzoyl]benzoic acid is a chemical compound with a complex structure. It contains a benzoylbenzoic acid core with a hydroxyl group and a dibutylamino substituent. 2-[4-(Dibutylamino)-2-hydroxybenzoyl]benzoic acid is used in pharmaceutical research and may have potential applications as a drug or drug intermediate. It is a white to light yellow solid and has a molecular weight of 402.51 g/mol. Its precise function and specific uses would depend on further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 54574-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,7 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54574-82:
(7*5)+(6*4)+(5*5)+(4*7)+(3*4)+(2*8)+(1*2)=142
142 % 10 = 2
So 54574-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C22H27NO4/c1-3-5-13-23(14-6-4-2)16-11-12-19(20(24)15-16)21(25)17-9-7-8-10-18(17)22(26)27/h7-12,15,24H,3-6,13-14H2,1-2H3,(H,26,27)

54574-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(Dibutylamino)-2-Hydroxybenzoyl]Benzoic Acid

1.2 Other means of identification

Product number -
Other names 2-[4-(Dibutylamino)-2-hydroxybenzoyl]benzoic 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:54574-82-2 SDS

54574-82-2Relevant articles and documents

Syntheses and photophysical properties of aminobenzopyranoxanthene dyes containing various alkyl chains at amine moieties

Kamino, Shinichiro,Tanioka, Masaru,Sawada, Daisuke,Enomoto, Shuichi

, p. 1167 - 1176 (2019/12/11)

Aminobenzopyranoxanthene (ABPX) dyes containing linear n-alkyl chains at amino groups were synthesized, and their cis and trans stereoisomers were isolated. Detailed spectrophotometric studies revealed that all the ABPX derivatives exhibited fluorescence emission in the far-red and near-infrared wavelength regions, and their fluorescence quantum efficiency increased with increasing n-alkyl chain length. Almost no differences in photophysical properties were observed between the cis and trans stereoisomers.

A new class of rhodamine luminophores: Design, syntheses and aggregation-induced emission enhancement

Kamino, Shinichiro,Horio, Yuka,Komeda, Seiji,Minoura, Katsuhiko,Ichikawa, Hayato,Horigome, Jun,Tatsumi, Asana,Kaji, Shinya,Yamaguchi, Takako,Usami, Yoshihide,Hirota, Shun,Enomoto, Shuichi,Fujita, Yoshikazu

supporting information; experimental part, p. 9013 - 9015 (2011/02/16)

A new class of rhodamine luminophores, 3′,3″- bis(oxospiroisobenzofuran)-3,7-bis(dialkylamino)benzopyrano-xanthene derivatives (ABPX), have been successfully developed. The emission behavior of ABPX series is directly opposite to the concentration quenching of conventional rhodamine dyes. ABPX series exhibit aggregation-induced emission enhancement (AIEE).

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