콘텐츠로 건너뛰기
Merck
모든 사진(1)

Key Documents

532576

Sigma-Aldrich

Chromone-3-carboxylic acid

97%

로그인조직 및 계약 가격 보기


About This Item

실험식(Hill 표기법):
C10H6O4
CAS Number:
Molecular Weight:
190.15
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

97%

mp

202-205 °C (lit.)

SMILES string

OC(=O)C1=COc2ccccc2C1=O

InChI

1S/C10H6O4/c11-9-6-3-1-2-4-8(6)14-5-7(9)10(12)13/h1-5H,(H,12,13)

InChI key

PCIITXGDSHXTSN-UHFFFAOYSA-N

유전자 정보

human ... PTPN1(5770)

일반 설명

Chromone-3-carboxylic acid is a chromone derivative. Its potential as an antioxidant in charge transfer (CT) processes has been assessed by surface-enhanced Raman scattering (SERS) analysis of chromone 3-carboxylic acid adsorbed on silver colloids.

애플리케이션

Chromone-3-carboxylic acid may be used in the preparation of:
  • chromane-2,4-diones
  • chromone-3-carboxamides
  • 5-(2-hydroxyphenyl)isoxazole
  • chromone-2-carboxamides
  • chromone-2-carboxamido-3-esters

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Conjugate addition of isocyanides to chromone 3-carboxylic acid: an efficient one-pot synthesis of chroman-4-one 2-carboxamides.
Neo AG, et al.
Organic & Biomolecular Chemistry, 10(17), 3406-3416 (2012)
Chromone-3-carboxylic acid as a potential electron scavenger: a surface-enhanced Raman scattering study.
Machado NFL, et al.
Physical Chemistry Chemical Physics, 13(3), 1012-1018 (2011)
F Cagide et al.
Chemical communications (Cambridge, England), 51(14), 2832-2835 (2015-01-13)
The discovery of potent and selective monoamine oxidase-B inhibitors for the management of neurodegenerative diseases such as Alzheimer's and Parkinson's diseases is still a challenging endeavor. Herein, we report the discovery of two new classes of potent and selective MAO-B
Synthesis of [1] benzopyrano [3,4-d] isoxazol-4-ones from 2-substituted chromone-3-carboxylic esters. A reinvestigation of the reaction of 3-acyl-4-hydroxycoumarins with hydroxylamine. Synthesis of 4-(2-hydroxybenzoyl) isoxazol-5-ones.
Chantegrel B, et al.
The Journal of Organic Chemistry, 49(23), 4419-4424 (1984)

자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..

고객지원팀으로 연락바랍니다.