추천 제품
분석
98%
형태
powder
mp
212-213 °C (dec.) (lit.)
SMILES string
Cn1c(cc2ccccc12)C(O)=O
InChI
1S/C10H9NO2/c1-11-8-5-3-2-4-7(8)6-9(11)10(12)13/h2-6H,1H3,(H,12,13)
InChI key
MAHAMBLNIDMREX-UHFFFAOYSA-N
일반 설명
1-Methylindole-2-carboxylic acid reacts with thionyl chloride to yield sulfinyl chlorides.
애플리케이션
- Reactant for preparation of keto-indoles as novel indoleamine 2,3-dioxygenase (IDO) inhibitors
- Reactant for synthesis of fenbufen and ethacrynic acid derivatives as potential antitumor agents via amide coupling reactions
- Reactant for diastereoselective synthesis of vinylated heterocycles via ruthenium-catalyzed oxidative vinylation with alkenes
- Reactant for synthesis of 2,3-dihalo indoles via hypervalent iodine mediated decarboxylative halogenation
- Reactant for preparation of α-ketoamides as cathepsin S inhibitors with potential applications against tumor invasion and angiogenesis
- Reactant for preparation of anthranilic acid mimics as bacterial translation inhibitors
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Reaction of Indole Derivatives with Thionyl and Sulfuryl Chlorides.
The Journal of Organic Chemistry, 29(1), 178-184 (1964)
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