(S)-2-(4-플루오로페닐)피롤리딘

(S)-2-(4-플루오로페닐)피롤리딘
(S)-2-(4-플루오로페닐)피롤리딘 구조식 이미지
카스 번호:
298690-90-1
한글명:
(S)-2-(4-플루오로페닐)피롤리딘
동의어(한글):
(S)-2-(4-플루오로페닐)피롤리딘
상품명:
(S)-2-(4-Fluorophenyl)pyrrolidine
동의어(영문):
(S)-2-(4-Fluorophenyl)pyrrolidine;(2S)-2-(4-fluorophenyl)pyrrolidine;Pyrrolidine, 2-(4-fluorophenyl)-, (2S)-;(S)-2-(4-Fluorophenyl)pyrrolidine (S)-2-(4-Fluorophenyl)pyrrolidine
CBNumber:
CB9875223
분자식:
C10H12FN
포뮬러 무게:
165.21
MOL 파일:
298690-90-1.mol

(S)-2-(4-플루오로페닐)피롤리딘 속성

끓는 점
235.5±33.0 °C(Predicted)
밀도
1.078±0.06 g/cm3(Predicted)
저장 조건
under inert gas (nitrogen or Argon) at 2–8 °C
산도 계수 (pKa)
9.76±0.10(Predicted)
CAS 데이터베이스
298690-90-1(CAS DataBase Reference)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
HS 번호 2933998090
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H315 피부에 자극을 일으킴 피부부식성 또는 자극성물질 구분 2 경고 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 호흡 자극성을 일으킬 수 있음 특정 표적장기 독성 - 1회 노출;호흡기계 자극 구분 3 경고 GHS hazard pictograms
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.

(S)-2-(4-플루오로페닐)피롤리딘 C화학적 특성, 용도, 생산

용도

(S)-2-(4-Fluorophenyl)pyrrolidine is a pyrrole compound and can be used in the synthesis of organic compounds.

주요 응용

(S)-2-(4-Fluorophenyl)pyrrolidine, also known as amide 2-(4-fluorophenyl)-2-pyrrolidinone, is a drug that has been discovered but not yet clinically developed. It is a blocker of the atrial natriuretic peptide receptor.

Synthesis

The mixture of tert-butyl (4-(4-fluorophenyl)-4-oxobutyl)carbamate (0.2 mmol) and trifluoroacetic acid (equiv) in CH2Cl2 was stirred under nitrogen for 3 h. After all the acid and solvent had been removed under vacuum, the obtained substance was transferred to a nitrogen-filled glovebox and dissolved in a mixed solvent of toluene/THF (5:1, 1 mL). Ti(OiPr)4 (0.24 mmol), DABCO (0.04 mmol), Ir-L9 (0.002 mmol) and KI (0.04 mmol) were added subsequently to the above solution. The total solution was made to 3.0 mL. The resulting vial was transferred to an autoclave, which was charged with 50 atm of H2, and stirred at 50 °C for 13 h. The solution was quenched with aqueous sodium bicarbonate solution. The organic phase was concentratedand the metal complex was removed by using a short silica plug to give the (S)-2-(4-Fluorophenyl)pyrrolidine.

(S)-2-(4-플루오로페닐)피롤리딘 준비 용품 및 원자재

원자재

준비 용품


(S)-2-(4-플루오로페닐)피롤리딘 공급 업체

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