推薦產品
品質等級
化驗
98%
mp
45-48 °C (lit.)
SMILES 字串
Fc1ccc2[nH]ccc2c1
InChI
1S/C8H6FN/c9-7-1-2-8-6(5-7)3-4-10-8/h1-5,10H
InChI 密鑰
ODFFPRGJZRXNHZ-UHFFFAOYSA-N
尋找類似的產品？ 前往 產品比較指南
應用
- 用于制备 5-HT6 受体配体
- 作为反应物，用于制备色氨酸双加氧酶抑制剂吡啶基-乙烯基-吲哚（一种潜在的抗癌免疫调节剂）
- 用于制备抗肿瘤药物的反应物
- 用于制备抗菌剂的反应物
- 用于制备免疫抑制剂的反应物
- 用于制备钠依赖性葡萄糖协同转运蛋白 2 (SGLT2) 抑制剂的反应物，用于治疗糖尿病高血糖症
- 用于制备髓过氧化物酶抑制剂的反应物
- 用于制备强效选择性 5-羟色胺再摄取抑制剂的反应物
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
230.0 °F - closed cup
閃點（°C）
110 °C - closed cup
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
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A practical synthesis of the glycogen synthase kinase-3 (GSK3) inhibitor bisarylmaleimide 1 has been accomplished employing Pictet-Spengler methodology to access the indole 7-position in preparing the benzodiazepine tricyclic fragment. A seven-step linear sequence that starts with commercially available 5-fluoroindole 7
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A J Barczak et al.
Genetics, 140(1), 303-313 (1995-05-01)
A study of the biochemical genetics of the Arabidopsis thaliana tryptophan synthase beta subunit was initiated by characterization of mutants resistant to the inhibitor 5-fluoroindole. Thirteen recessive mutations were recovered that are allelic to trp2-1, a mutation in the more
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