3,4-디메톡시페놀

3,4-디메톡시페놀
3,4-디메톡시페놀 구조식 이미지
카스 번호:
2033-89-8
한글명:
3,4-디메톡시페놀
동의어(한글):
3,4-디메톡시페놀
상품명:
3,4-Dimethoxyphenol
동의어(영문):
NSC 140927;3,4-Dimethoxyphel;4-HYDROXYVERATROLE;3,4-DIMETHOXYPHENOL;3,4-dimethoxy-pheno;3,4-diMethoxyphenoxyl;Phenol, 3,4-dimethoxy-;3,4-Dimethoxyphenol,97%;3,4-Dimethoxyphenol >3,4-Bis(Methyloxy)phenol
CBNumber:
CB2354549
분자식:
C8H10O3
포뮬러 무게:
154.16
MOL 파일:
2033-89-8.mol
MSDS 파일:
SDS

3,4-디메톡시페놀 속성

녹는점
79-82 °C (lit.)
끓는 점
167°C/14mm
밀도
1.1690 (rough estimate)
굴절률
1.4740 (estimate)
인화점
167°C/14mm
저장 조건
Keep in dark place,Inert atmosphere,Room temperature
용해도
클로로포름(약간 용해됨), 메탄올(약간 용해됨)
산도 계수 (pKa)
10.08±0.18(Predicted)
물리적 상태
미세 결정성 분말
색상
미색부터 밝은 베이지까지
수용성
물에 용해됩니다.
감도
Light Sensitive
BRN
1366650
LogP
1.157 (est)
CAS 데이터베이스
2033-89-8(CAS DataBase Reference)
NIST
Phenol, 3,4-dimethoxy-(2033-89-8)
EPA
3,4-Dimethoxyphenol (2033-89-8)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi
위험 카페고리 넘버 36/37/38
안전지침서 26-36-37/39
WGK 독일 3
F 고인화성물질 10
TSCA Yes
HS 번호 29095000
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:
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
1
2 0

3,4-디메톡시페놀 MSDS


3,4-Dimethoxyphenol

3,4-디메톡시페놀 C화학적 특성, 용도, 생산

화학적 성질

Red Crystal Powder

용도

3,4-Dimethoxyphenol is used in the preparation of 5,6-dimethoxy benzofuranone derivatives and multi-target anti Alzheimer compounds. It is also used in the preparation of 3,4-dimethoxyphenyl-beta-D-glucopyranoside and 4-(but-2-enyloxy)-1,2-dimethoxybenzene. Further, it serves as a precursor for 4H-chromenes synthesis.

Synthesis

3,4-Dimethoxyphenol is synthesised using Veratraldehyde as a raw material by chemical reaction. The specific synthesis steps are as follows:
Method (i): To a solution of vertraldehyde (2.11)(5 g,0.03 mole)in glacial acetic acid (30 ml)is added dropwise to a solution of peracetic acid5(15 ml) during 30 min.The temperature of the reaction mixture rises,it is kept at 40-45 by cooling.The reaction mixture is left for 10 hr and then concentrated to about 15 ml in vacuo.The residue is extracted with ether (2 x 20 ml).The ether layer is distilled.The formate ester of 3,4- dimethoxyphenol thus obtained is hydrolysed by refluxing with potassium hydroxide (10 g)in aqueous alcohol (1:4,100 ml)for 1 hr.The reaction mixture is concentrated in vacuo almost to dryness.It is dissolved in water (20 ml),the solution rendered acidic with dilute sulphuric acid and extracted with ether.The ether extract is dried (sodium sulphate)and distilled.The oily residue thus obtained is subjected to column chromatography over silica gel(2 x 30 cm).Elution with benzene gave 3,4-dimethoxyphenol as yellow solid.Yield 3g(65.2%).It is crystallised from  benzene as yellow crystalline needles.M.p.78-80(lit.m.p.78-80).
3,4-Dimethoxyphenol synthesis 1
Method (ii): A mixture of veratraldehyde (2.11)(1.66 g,0.01 mole),hydrogen peroxide (30%,2.6 ml,0.023 mole),p-toluenesulphonic acid (6.88 g, 0.036 mole)and methanol (5 ml)is stirred at room temperature.When the reaction is complete (as monitored by TLC)the reaction mixture is diluted with water (50 ml)and extracted with dichloromethane (5 x 50 ml).The extract is dried (anhydrous sodium sulphate)and purified by column chromatography over silica gel(2 x 30 cm).Elution with benzene gave 3,4. dimethoxyphenol as an yellow solid.Yield 1.16 g (75.3%).M.p.78-80.
3,4-Dimethoxyphenol synthesis 2

3,4-디메톡시페놀 준비 용품 및 원자재

원자재

준비 용품


3,4-디메톡시페놀 공급 업체

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