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2- 메틸 린돌 -3- 카 복스 알데히드메이커 CAS 레지스트리 번호5416-80-8공급업체 | LookChem

2- 메틸 린돌 -3- 카 복스 알데히드

기본 정보 Edit
  • 표준명:2- 메틸 린돌 -3- 카 복스 알데히드
  • CAS 레지스트리 번호:5416-80-8
  • 분자식:C
  • 분자 무게:159.188
  • HS 코드:2933.99
  • Mol 파일:5416-80-8.mol
2- 메틸 린돌 -3- 카 복스 알데히드

동의어: 2-methyl-1h-indole-3-carboxaldehyd;3-FORMYL-2-METHYLINDOLE;AKOS BBS-00000868;AKOS JY2083591;AKOS 233-93;2-METHYLINDOLE-3-CARBALDEHYDE;2-METHYLINDOLE-3-CARBOXALDEHYDE;2-METHYLINDOLE-3-CARBOXYALDEHYDE

관련 CAS 번호: 51325-39-4 59551-02-9 57647-79-7 53629-19-9 53342-23-7 50876-23-8 58793-45-6 58881-45-1 55154-18-2 58759-02-7

표준명의 마케팅 및 가격
제조업체 및 유통업체:
  • 제조/브랜드
  • 화학물질 및 원자재
  • 포장
  • 가격
  • TCI Chemical
  • 2-Methylindole-3-carboxaldehyde >98.0%(GC)
  • 25g
  • $ 149.00
  • TCI Chemical
  • 2-Methylindole-3-carboxaldehyde >98.0%(GC)
  • 5g
  • $ 48.00
  • SynQuest Laboratories
  • 2-Methyl-1H-indole-3-carboxaldehyde
  • 5 g
  • $ 77.00
  • SynQuest Laboratories
  • 2-Methyl-1H-indole-3-carboxaldehyde
  • 1 g
  • $ 16.00
  • SynChem
  • 2-Methyl-1H-indole-3-carbaldehyde 95%
  • 1 g
  • $ 15.00
  • SynChem
  • 2-Methyl-1H-indole-3-carbaldehyde 95%
  • 5 g
  • $ 30.00
  • Sigma-Aldrich
  • 2-Methylindole-3-carboxaldehyde 97%
  • 25g
  • $ 98.00
  • Medical Isotopes, Inc.
  • 2-Methyl-1H-indole-3-carbaldehyde 95+%
  • 10 g
  • $ 355.00
  • Matrix Scientific
  • 2-Methyl-1H-indole-3-carbaldehyde
  • 100g
  • $ 265.00
  • Matrix Scientific
  • 2-Methyl-1H-indole-3-carbaldehyde
  • 25g
  • $ 78.00
총 81 개 원재료 공급업체
표준명의 화학적 성질 Edit
물리적 데이터:
안전정보:
  • 픽토그램: IrritantXi
  • 위험 코드: Xi
  • 진술: 36/37/38
  • 안전 선언문: S26-S37/39
사용:
  • 소개 및 적용: 2-Methyl indole-3-carboxaldehyde is a versatile reactant used in the preparation of various compounds, including Tryptophan dioxygenase inhibitors, pyridyl-ethenyl-indoles, which have potential as anticancer immunomodulators, fluorescent sensors (BODIPY), antimicrobial agents against methicillin-resistant Staphylococcus aureus, G protein-coupled receptor CRTh2 antagonists, inhibitors of PI3 kinase-α, antitubercular agents, anti-inflammatory agents, Mycobacterium tuberculosis protein tyrosine phosphatase B, glucocorticoid receptor ligands, and agents that stimulate neurite outgrowth. The oxidative activation of 2-methylindole-3-carboxaldehyde via N-heterocyclic carbene organocatalysis generates heterocyclic ortho-quinodimethane as a key intermediate, which can be used in the synthesis of these diverse compounds.
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