2-나프탈레놀,3-브로모-

2-나프탈레놀,3-브로모-
2-나프탈레놀,3-브로모- 구조식 이미지
카스 번호:
30478-88-7
한글명:
2-나프탈레놀,3-브로모-
동의어(한글):
2-나프탈레놀,3-브로모-
상품명:
3-Bromo-2-naphthol
동의어(영문):
3-Bromo-2-naphthol;3-Bromo-2-naphthol >3-bromo-2-naphthalenol;3-Bromo-2-naphthol 99%;3-broMonaphthalen-2-ol;2-NAPHTHALENOL, 3-BROMO-;2-NAPHTHALENOL, 3-BROMO- ISO 9001:2015 REACH
CBNumber:
CB21474099
분자식:
C10H7BrO
포뮬러 무게:
223.07
MOL 파일:
30478-88-7.mol
MSDS 파일:
SDS

2-나프탈레놀,3-브로모- 속성

녹는점
82 °C
끓는 점
313.7±15.0 °C(Predicted)
밀도
1.614±0.06 g/cm3(Predicted)
저장 조건
Keep in dark place,Inert atmosphere,Room temperature
물리적 상태
powder to crystal
산도 계수 (pKa)
8.03±0.40(Predicted)
색상
흰색에서 밝은 노란색
CAS 데이터베이스
30478-88-7
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi
위험 카페고리 넘버 37/38-41
안전지침서 26-39
WGK 독일 3
HS 번호 2908.19.6000
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Danger
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
H318 눈에 심한 손상을 일으킴 심한 눈 손상 또는 자극성 물질 구분 1 위험 GHS hazard pictograms P280, P305+P351+P338, P310
H335 호흡 자극성을 일으킬 수 있음 특정 표적장기 독성 - 1회 노출;호흡기계 자극 구분 3 경고 GHS hazard pictograms
예방조치문구:
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
NFPA 704
0
2 0

2-나프탈레놀,3-브로모- C화학적 특성, 용도, 생산

Synthesis

3-Bromo-2-naphthol is synthesised using 2-bromo-3-methoxynaphthalene as a raw material by chemical reaction. The specific synthesis steps are as follows:
General procedure: To a Schlenk flask were added 2-bromo-3-methoxynaphthalene(1.0 equiv), aryl boronic acid (2.2 equiv), K2CO3 (3.0 equiv), Pd(PPh3)4 (2.5 mol%), and degassed EtOH/toluene/water (1/1/1) under Ar atmosphere. The mixture was heated at 90 °C until thecompletion of the reaction. Then the mixture was cooled to room temperature, and DCM was added. The mixture was washed with NaOH solution (20% wt), and the aqueous phase was extracted with DCM (2 × 20 mL). The combined organic phase was washed with brine (20 mL) and dried overanhydrous MgSO4. After removing the solvent, the residue was dissolved in anhydrous DCM. Thesolution was cooled to -78 °C, and BBr3 (1 M in DCM, 5.0 equiv) was added slowly by syringe. Thenthe mixture was warmed up to room temperature and stirred until the complete consumption of thestarting material. The mixture was poured into the ice water (50 mL) and extracted with DCM (3 × 50mL). The combined organic phase was washed with brine (100 mL) and dried over anhydrous Na2SO4. After removing the solvent, the residue was purified by silica gel chromatography to give 3-Bromo-2-naphthol.
3-Bromo-2-naphthol synthesis

2-나프탈레놀,3-브로모- 준비 용품 및 원자재

원자재

준비 용품


2-나프탈레놀,3-브로모- 공급 업체

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