추천 제품
분석
98%
refractive index
n20/D 1.5170 (lit.)
bp
138 °C (lit.)
density
1.039 g/mL at 25 °C (lit.)
작용기
fluoro
SMILES string
Fc1cccc(c1)C#C
InChI
1S/C8H5F/c1-2-7-4-3-5-8(9)6-7/h1,3-6H
InChI key
PTRUTZFCVFUTMW-UHFFFAOYSA-N
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
90.0 °F - closed cup
Flash Point (°C)
32.2 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
Lot/Batch Number
이미 열람한 고객
Jason Manka et al.
Probe Reports from the NIH Molecular Libraries Program, 2011 Dec 16 (Updated 2013 Mar 7) (2013-06-14)
Allosteric modulators for G-protein-coupled receptors (GPCRs) provide numerous advantages over orthosteric ligands, including greater sub-type selectivity, reduced receptor desensitization, saturability of effect, and potential for enhanced therapeutic index. Positive allosteric modulators (PAMs) of the group I metabotropic glutamate receptor mGlu
(NHC) Copper (I)-Catalyzed [3+ 2] Cycloaddition of Azides and Mono-or Disubstituted Alkynes.
Diez-Gonzalez S, et al.
Chemistry (Weinheim An Der Bergstrasse, Germany), 12(29), 7558-7564 (2006)
Chunfa Xu et al.
Angewandte Chemie (International ed. in English), 53(35), 9316-9320 (2014-07-22)
A new, electrophilic trifluoromethylthiolating reagent, N-trifluoromethylthiosaccharin, was developed and can be synthesized in two steps from saccharin within 30 minutes. N-trifluoromethylthiosaccharin is a powerful trifluoromethylthiolating reagent and allows the trifluoromethylthiolation of a variety of nucleophiles such as alcohols, amines, thiols, electron-rich
Ya Zhou et al.
Probe Reports from the NIH Molecular Libraries Program, 2011 Oct 31 (Updated 2013 Mar 7) (2013-06-14)
A series of acetylenic biaryl mGlu5 positive allosteric modulators (PAMs) have been optimized as pure potentiators in low receptor expressing mGlu5 cell lines. ML254 was identified and shown to competitively interact with the MPEP allosteric binding site. Preliminary data from
Lei Zhou et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(43), 11668-11674 (2009-09-25)
A simple and efficient method for the synthesis of gamma,delta-alkynyl-beta-amino acid derivatives by a copper-catalyzed three-component amine-alkyne-alkyne addition reaction was developed. Various gamma,delta-alkynyl-beta-amino acid derivatives were synthesized in moderate to good yields in one step. With chiral prolinol derivatives employed
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