벤조티아졸

벤조티아졸
벤조티아졸 구조식 이미지
카스 번호:
95-16-9
한글명:
벤조티아졸
동의어(한글):
벤조싸이아졸;벤조티아졸
상품명:
Benzothiazole
동의어(영문):
Benzo[d]thiazole;Benzothiazol;1,3-BENZOTHIAZOLE;Vangard BT;o-2857;NSC 8040;vangardbt;FEMA 3256;usafek-4812;USAF ek-4812
CBNumber:
CB1720657
분자식:
C7H5NS
포뮬러 무게:
135.19
MOL 파일:
95-16-9.mol
MSDS 파일:
SDS

벤조티아졸 속성

녹는점
2 °C (lit.)
끓는 점
231 °C (lit.)
밀도
1.238 g/mL at 25 °C (lit.)
증기 밀도
4.66 (vs air)
증기압
34 mm Hg ( 131 °C)
굴절률
n20/D 1.642(lit.)
FEMA
3256 | BENZOTHIAZOLE
인화점
>230 °F
저장 조건
Keep in dark place,Inert atmosphere,Room temperature
용해도
3g/L
물리적 상태
액체
산도 계수 (pKa)
0.85±0.10(Predicted)
색상
투명한 황갈색~갈색
냄새
퀴놀린 냄새, 약간의 물-졸 냄새
?? ??
유황의
폭발한계
0.9-8.2%(V)
수용성
약간 용해됨
Merck
14,1107
JECFA Number
1040
BRN
109468
안정성
안정적 - 환경에 대한 지속성이 매우 높은 것으로 간주됩니다. 강한 산화제와 호환되지 않습니다. 연소 생성물: 질소 산화물, 일산화탄소, 이산화탄소, 황산화물.
InChIKey
IOJUPLGTWVMSFF-UHFFFAOYSA-N
LogP
2.01
CAS 데이터베이스
95-16-9(CAS DataBase Reference)
NIST
Benzothiazole(95-16-9)
EPA
Benzothiazole (95-16-9)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,T,Xi
위험 카페고리 넘버 22-20/21/22-36-25-24-20
안전지침서 23-26-36-36/37-45
유엔번호(UN No.) 2810
WGK 독일 2
RTECS 번호 DL0875000
TSCA Yes
위험 등급 6.1
포장분류 III
HS 번호 29342080
유해 물질 데이터 95-16-9(Hazardous Substances Data)
독성 LD50 i.v. in mice: 95±3 mg/kg (Domino)
기존화학 물질 KE-02722
그림문자(GHS): GHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
예방조치문구:
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P301+P310 삼켰다면 즉시 의료기관(의사)의 진찰을 받으시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
1
2 0

벤조티아졸 MSDS


Benzothiazole

벤조티아졸 C화학적 특성, 용도, 생산

개요

Benzothiazole and its derivative are recognized as the most important heterocyclic compounds. This series of compounds is of particular interests. It has various kinds of pharmacological properties and has been included in many kinds of natural products and pharmaceutical agents. The broad spectrum of pharmacological activity in individual benzothiazole derivative enables it to serve as unique and valuable scaffolds for experimental drug design. It is already known that benzothiazole and its derivative has various biological applications including anticancer, antimicrobial, anticonvulsant, antiviral, antidiabetic, antipsychotic, antiinflammatory, analgesic, fungicidal and diuretic. Its derivatives also have many applications in polymer chemistry, dyes, drugs, and silver photography as well as rubber industry.

화학적 성질

Benzothiazole has a delicate, persistent, rose-like odor similar to that of quinoline.

출처

Reported found in apricot, cooked asparagus, mozzarella cheese, skim milk powder, roasted beef, beer, malt whiskey, coconut meat, fresh mango, cooked broccoli and kelp.

용도

Various benzothiazole-benzamides synthesized were evaluated for their analgesic and antidepressant activities.

정의

ChEBI: An organic heterobicyclic compound that is a fusion product between benzene and thiazole. The parent of the class of benzothiazoles.

제조 방법

By refluxing a mixture of zinc o-aminophenylsulfide and formic acid, followed by steam distillation of the alkalized reaction mixture; by heating formanilid or dimethylaniline with sulfur; by oxidation of 2-mercaptobenzothiazole or of the corresponding disulfide.

일반 설명

Benzothiazole, a volatile sulfur-containing heterocyclic compound, is one of the key odorants of heated milk. It is also reported to occur as a flavor component of miso, coconut meat and cooked-beef.

위험도

Highly toxic by ingestion.

Safety Profile

Poison by ingestion,intraperitoneal, intravenous, and possibly other routes.When heated to decomposition it emits very toxic fumesof SOx, CN??, and NOx.

참고 문헌

Gupta, Akhilesh, and S. Rawat. "Synthesis and cyclization of benzothiazole." J. of Current Pharmaceutical Research 3.1 (2010): 13-25.
Keri, Rangappa S., et al. "A comprehensive review in current developments of benzothiazole-based molecules in medicinal chemistry." European journal of medicinal chemistry 89 (2015): 207-251.
Khokra, Sukhbir L., et al. "Common methods to synthesize benzothiazole derivatives and their medicinal significance: a review." International Journal of Pharmaceutical Sciences and Research 2.6 (2011): 1356.

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