1-Fluoronaphthalene

1-Fluoronaphthalene 구조식 이미지
카스 번호:
321-38-0
상품명:
1-Fluoronaphthalene
동의어(영문):
Fluoronaphthalene;1-FLUORONAPTHALENE;1-Fluornaftalen;48720-u;NSC 4690;uoronaphthaL;Duloxetine-8;1-Fluoronaphth;Fluorophthalene;Duloxetine Imp-G
CBNumber:
CB8219439
분자식:
C10H7F
포뮬러 무게:
146.16
MOL 파일:
321-38-0.mol
MSDS 파일:
SDS

1-Fluoronaphthalene 속성

녹는점
-13 °C (lit.)
끓는 점
215 °C (lit.)
밀도
1.1322 g/mL at 20 °C (lit.)
굴절률
n20/D 1.593(lit.)
인화점
150 °F
저장 조건
Sealed in dry,Room Temperature
용해도
물에 약간 용해되고 클로로포름, 에틸 아세테이트 및 메탄올에 잘 용해됩니다.
물리적 상태
기름
색상
무색~황색
Specific Gravity
1.332
수용성
물에 섞이거나 혼합하기 어렵지 않습니다.
BRN
1906413
안정성
안정적인. 강한 산화제와 호환되지 않습니다.
InChIKey
CWLKTJOTWITYSI-UHFFFAOYSA-N
CAS 데이터베이스
321-38-0(CAS DataBase Reference)
NIST
Naphthalene, 1-fluoro-(321-38-0)
EPA
1-Fluoronaphthalene (321-38-0)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi
위험 카페고리 넘버 36/37/38
안전지침서 26-36
유엔번호(UN No.) UN2810
WGK 독일 3
RTECS 번호 QJ7100000
위험 참고 사항 Flammable
TSCA T
위험 등급 IRRITANT
HS 번호 29039990
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.
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P271 옥외 또는 환기가 잘 되는 곳에서만 취급하시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
2
1 0

1-Fluoronaphthalene MSDS


Fluoronaphthalene

1-Fluoronaphthalene C화학적 특성, 용도, 생산

화학적 성질

clear slightly yellow to yellow-brown liquid

용도

1-Fluoronaphthalene is a fluorinated naphthalene derivative that is metabolized by fungal monooxygenase-epoxide hydrolase. It is also used as a pharmaceutical intermediate. It is Duloxetine impurity.

주요 응용

1-Fluoronaphthalene was used in t-BuLi-mediated synthesis of 6-substituted phenanthridines. It was also used in the synthesis of LY248686, a potent inhibitor of serotonin and norepinephrine uptake.

제조 방법

The preparation of 1-Fluoronaphthalene is as follows:1) Diazotization reaction: 1500 g of hydrochloric acid (mass concentration: 25%) and 300 g of naphthylamine were added to a 3000 mL three-necked flask, stirred and heated to 75 ° C to dissolve, and the temperature was lowered to below 5 ° C, and 148 g was slowly added at this temperature. Sodium nitrite, stirred at low temperature for 0.3 hours after the addition, to obtain a diazonium salt solution;2) Substitution reaction: 360 g of fluoroboric acid solution (concentration: 45%) was added to the resulting solution obtained in the step 1), stirred for 0.25 h, filtered, and the filter cake was dried at a temperature of 50 ° C for 0.2 h to obtain Dry naphthylamine diazonium salt fluoroborate double salt;3) Hot air decomposition: the dried diazonium salt fluoroborate double salt is slowly added to the reactor through which hot air (hot air temperature is 85-90 ° C), and the dried powdered naphthylamine diazonium salt fluoroborate double salt is The hot air blows up the dispersion and absorbs the heat for thermal decomposition to obtain a 1-fluoronaphthalene solution containing a small amount of solid impurities;4) Purification treatment: the 1-fluoronaphthalene solution obtained in the step 3) is first washed with pure water for 3 to 6 times, then neutralized with a soda ash to a pH of 6.8 to 7.2, and finally the oil layer is separated by filtration, and the filtrate is taken. The distillation treatment gave 210 g of a naphthalene-based fluorine-containing intermediate 1-fluoronaphthalene in an amount of 99.8%.

321-38-0.png

공기와 물의 반응

Insoluble in water.

반응 프로필

Simple aromatic halogenated organic compounds, such as Fluoronaphthalene, are very unreactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Materials in this group may be incompatible with strong oxidizing and reducing agents. Also, they may be incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.

1-Fluoronaphthalene 준비 용품 및 원자재

원자재

준비 용품


1-Fluoronaphthalene 공급 업체

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