2-티오페네카르복스알데하이드

2-티오페네카르복스알데하이드
2-티오페네카르복스알데하이드 구조식 이미지
카스 번호:
98-03-3
한글명:
2-티오페네카르복스알데하이드
동의어(한글):
2-티오펜카복스알데하이드;2-티오페네카르복스알데하이드
상품명:
2-Thiophenecarboxaldehyde
동의어(영문):
THIOPHENE-2-CARBALDEHYDE;2-THIOPHENECARBOXALDEHYDE;THIOPHENE-2-ALDEHYDE;THIOPHENE-2-CARBOXALDEHYDE;2-THIOPHENECARBALDEHYDE;formylthiophene;S0508;2-Thienal;2-Theldehyde;THENALDEHYDE
CBNumber:
CB2488611
분자식:
C5H4OS
포뮬러 무게:
112.15
MOL 파일:
98-03-3.mol
MSDS 파일:
SDS

2-티오페네카르복스알데하이드 속성

녹는점
<10°C
끓는 점
198 °C (lit.) 75-77 °C/11 mmHg (lit.)
밀도
1.2 g/mL at 25 °C (lit.)
굴절률
n20/D 1.591(lit.)
인화점
172 °F
저장 조건
2-8°C
용해도
클로로포름(약간 용해됨), DMSO(약간 용해됨), 에틸아세테이트(약간 용해됨)
물리적 상태
액체 (투명)
Specific Gravity
1.2
색상
맑은 노란색
냄새
유황의
?? ??
유황의
수용성
불용성
감도
Air Sensitive
BRN
105819
InChIKey
CNUDBTRUORMMPA-UHFFFAOYSA-N
LogP
1.020
CAS 데이터베이스
98-03-3(CAS DataBase Reference)
NIST
2-Thiophenecarboxaldehyde(98-03-3)
EPA
2-Thiophenecarboxaldehyde (98-03-3)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,Xi
위험 카페고리 넘버 22-36/37/38-43
안전지침서 36/37/39-37-24-36-26
유엔번호(UN No.) UN 2810
WGK 독일 3
RTECS 번호 XM8135000
F 고인화성물질 9
위험 참고 사항 Irritant
TSCA Yes
HS 번호 29349990
기존화학 물질 98-3-1084
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
예방조치문구:
NFPA 704
1
2 0

2-티오페네카르복스알데하이드 MSDS


2-Formylthiophene

2-티오페네카르복스알데하이드 C화학적 특성, 용도, 생산

개요

2-Thiophenecarboxaldehyde, also known as alpha-formylthiophene or 2-thienylaldehyde, belongs to the class of organic compounds known as aryl-aldehydes. Aryl-aldehydes are compounds containing an aldehyde group directly attached to an aromatic ring. 2-Thiophenecarboxaldehyde is a sulfurous tasting compound. 2-Thiophenecarboxaldehyde has been detected, but not quantified in, asparagus (Asparagus officinalis). This could make 2-thiophenecarboxaldehyde a potential biomarker for the consumption of these foods. 2-Thiophenecarboxaldehyde is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites.

화학적 성질

clear yellow to light brown liquid

용도

Thiophene derivatives, introducing thenyl group into organic compounds.

주요 응용

2-Thenaldehyde(T2A) was originally used to produce a range of antihistamines, including methapyrilene, methaphenilene, and thenalidine. However, this usage has practically disappeared. The anthelmintic pyrantel is an important outlet for T2A, enhanced by new formulations and the development of the medicinal use of pyrantel beyond the original veterinary market. An important T2A derivative is the antihypertensive eprosartan (2-thiophenepropionic acid methyl ester), which acts as a selective angiotensin II receptor antagonist. ?Other pharmaceuticals containing T2A are azosemide a diuretic, and teniposide an antineoplastic.

정의

ChEBI: 2-Thiophenecarboxaldehyde is an aldehyde that is thiophene substituted by a formyl group at position 2. It has a role as a metabolite. It is a member of thiophenes and an aldehyde.

일반 설명

Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards

Synthesis

2-Thiophenecarboxaldehyde is prepared by the reaction of 2-Iodothiophene and carbon monoxide. The specific synthesis steps are as follows:
General procedure: A flask was charged with aryl iodide 1 (0.5 mmol), Pd(OAc)2 (2.4 mg, 0.01mmol), Na2CO3 (53.1 mg. 0.5 mmol), NaHCO3 (42.0 mg, 0.5 mmol), and PEG-400 (2 g) beforestandard cycles evacuation and backfilling with dry and pure carbon monoxide. Triethylsilane(162.8 μl, 1.0 mmol) was added successively. Then, the mixture was stirred at room temperaturefor the indicated time. At the end of the reaction, the reaction mixture was extracted with diethylether (3 × 10 mL). The organic phases were combined, and the volatile components wereevaporated under reduced pressure. The crude product was purified by column chromatography onsilica gel (petroleum ether / diethyl ether).
2-Thiophenecarboxaldehyde synthesis

Purification Methods

Wash it with 50% HCl and distil it under reduced pressure just before use. It has UV: 234nm (hexane). The Z-oxime has m 144o, 136-138o and 142o (H2O). [Beilstein

2-티오페네카르복스알데하이드 준비 용품 및 원자재

원자재

준비 용품


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