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5-METHOXY-2-METHYLINDOLE

5-METHOXY-2-METHYLINDOLE 구조식 이미지
카스 번호:
1076-74-0
상품명:
5-METHOXY-2-METHYLINDOLE
동의어(영문):
NSC 63817;AKOS JY2082626;5-Methoxy-2-methyindole;2-Methyl-5-Methoxyindole;5-METHOXY-2-METHYLINDOLE;Indole, 5-methoxy-2-methyl-;5-Methoxy-2-methylindole>5-Methoxy-2-methylindole 99%;1H-Indole, 5-methoxy-2-methyl-;5-Methoxy-2-methylindole, 99+%
CBNumber:
CB8174569
분자식:
C10H11NO
포뮬러 무게:
161.2
MOL 파일:
1076-74-0.mol

5-METHOXY-2-METHYLINDOLE 속성

녹는점
86-88 °C (lit.)
끓는 점
145 °C / 1.5mmHg
밀도
1.0840 (rough estimate)
굴절률
1.5200 (estimate)
저장 조건
Keep in dark place,Sealed in dry,Room Temperature
용해도
Soluble in methanol (very faint turbidity.)
산도 계수 (pKa)
17.28±0.30(Predicted)
물리적 상태
Crystalline Powder or Crystals
색상
White to light beige
InChIKey
VSWGLJOQFUMFOQ-UHFFFAOYSA-N
CAS 데이터베이스
1076-74-0(CAS DataBase Reference)
안전
  • 위험 및 안전 성명
위험품 표기 Xi
위험 카페고리 넘버 36/37/38
안전지침서 37/39-26
WGK 독일 3
위험 등급 IRRITANT
HS 번호 29339900
그림문자(GHS):
신호 어:
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
예방조치문구:
NFPA 704
1
2 0

5-METHOXY-2-METHYLINDOLE C화학적 특성, 용도, 생산

개요

5-methoxy-2-methylindole is a useful organic raw material. It can be used as the reactant in the preparation of indolylquinoxalines by condensation reactions, in preparation of alkylindoles via Ir-catalyzed reductive alkylation, in arylation reactions in the presence of a palladium acetate catalyst, in enantioselective Friedel-Crafts alkylation, as well as in stereo selective synthesis of cyclopentaindolones via stereoselective [3+2] cyclopentannulation. It is also employed in inhibiting the chlorinating activity of myeloperoxidase (MPO) and in the metabolic synthesis of acrylacetic acid anti-inflammatory synthesis.

화학적 성질

white to light beige crystalline powder or

용도

An indole derivative shown to be an effective inhibitor of the chlorinating activity of myeloperoxidase (MPO). Used in the metabolic synthesis of arylacetic acid antiinflammatory synthesis.

용도

reactant in preparation of indolylquinoxalines by condensation reactions1reactant in preparation of alkylindoles via Ir-catalyzed reductive alkylation2reactant in arylation reactions using a palladium acetate catalyst3reactant in enantioselective Friedel-Crafts alkylation4reactant in stereoselective synthesis of cyclopentaindolones via stereoselective [3+2] cyclopentannulation5

참고 문헌

https://www.alfa.com/en/catalog/B21348/
http://www.sigmaaldrich.com/catalog/product/aldrich/m15451?lang=en&region=US
https://pubchem.ncbi.nlm.nih.gov/compound/5-Methoxy-2-methylindole#section=2D-Structure

5-METHOXY-2-METHYLINDOLE 준비 용품 및 원자재

원자재

준비 용품


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