콘텐츠로 건너뛰기
Merck
모든 사진(1)

주요 문서

모든 문서 보기

529133

Sigma-Aldrich

1-Methoxy-2-naphthoic acid

97%

로그인조직 및 계약 가격 보기
모든 사진(1)

About This Item

Linear Formula:
CH3OC10H6CO2H
CAS Number:
883-21-6
Molecular Weight:
202.21
MDL number:
MFCD00094169
UNSPSC 코드:
12352100
PubChem Substance ID:
24877652
NACRES:
NA.22

분석

97%

mp

125-129 °C (lit.)

작용기

carboxylic acid

SMILES string

COc1c(ccc2ccccc12)C(O)=O

InChI

1S/C12H10O3/c1-15-11-9-5-3-2-4-8(9)6-7-10(11)12(13)14/h2-7H,1H3,(H,13,14)

InChI key

PMJACRPIWSINFF-UHFFFAOYSA-N

일반 설명

1-Methoxy-2-naphthoic acid can be prepared from 1-methoxynaphthalene.[1] 1-Methoxy-2-naphthoic acid can also be synthesized by reacting potassium tert-butoxide with 1-methoxynaphthalene and butyllithium in the presence of cyclohexane and tetrahydrofuran.[2] It undergoes reduction in the presence of lithium to afford tetrahydronaphthoic acid.[3]

애플리케이션

1-Methoxy-2-naphthoic acid may be used in the synthesis of 2-(1-methoxy-2-naphthyl)-4,4-dimethyl-2-oxazoline.[1] It may also be used in the synthesis of the following compounds:[4]
  • 1-sec-butyl-2-naphthoic acid
  • 1-tert-butyl-2-naphthoic acid
  • 1-ethyl-2-naphthoic acid
  • 1-vinyl-2-naphthoic acid
  • 1-phenyl-2-naphthoic acid
  • 1-(2,5-dimethylphenyl)-2-naphthoic acid
  • 2′-methoxy-[1,1′-binaphthalene]-2-carboxylic acid

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
MKBK0952V
01510HJ
05203MD
14011LI

적합한 버전을 찾을 수 없으신가요?

특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

COA 검색

이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Eva Castagnetti et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 8(4), 799-804 (2002-02-22)
Judged by its capacity to promote a hydrogen/metal permutation at an ortho position, the trifluoromethoxy group is superior to both the methoxy and trifluoromethyl groups. Moreover, like CF(3) and unlike OCH(3), OCF(3) exerts a long-range effect that still considerably lowers
Chemistry of aryloxazolines. Applications to the synthesis of lignan lactone derivatives.
Meyers AI and Avila WB.
The Journal of Organic Chemistry, 46(19), 3881-3886 (1981)
The metalation of 1-methoxynaphthalene with n-butyllithium.
Graybill BM and Shirley DA.
The Journal of Organic Chemistry, 31(4), 1221-1225 (1966)
Birch Reduction of 2-Naphthoic and of ortho-Methoxynaphthoic Acids.
Eliel EL and Hoover TE.
The Journal of Organic Chemistry, 24(7), 938-942 (1959)
Regadia Aissaoui et al.
The Journal of organic chemistry, 77(1), 718-724 (2011-11-24)
Substitution of an ortho-fluoro or methoxy group in 1- and 2-naphthoic acids furnishing substituted naphthoic acids occurs in good to excellent yields upon reaction with alkyl/vinyl/aryl organolithium and Grignard reagents, in the absence of a metal catalyst without the need

질문

후기

평점 값 없음

활성 필터

자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..

고객지원팀으로 연락바랍니다.