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3-HYDROXY-4-METHOXYCARBONYLPHENYLBORONIC ACID, 피나콜 에스테르메이커 CAS 레지스트리 번호1073371-99-9공급업체 | LookChem

3-HYDROXY-4-METHOXYCARBONYLPHENYLBORONIC ACID, 피나콜 에스테르

기본 정보 Edit
  • 표준명:3-HYDROXY-4-METHOXYCARBONYLPHENYLBORONIC ACID, 피나콜 에스테르
  • CAS 레지스트리 번호:1073371-99-9
  • 분자식:C14H19BO5
  • 분자 무게:278.113
  • HS 코드:2934999090
  • Mol 파일:1073371-99-9.mol
3-HYDROXY-4-METHOXYCARBONYLPHENYLBORONIC ACID, 피나콜 에스테르

동의어: 3-HYDROXY-4-METHOXYCARBONYLPHENYLBORNIC ACID, PINACOL ESTER;메틸 2-하이드록시-4-(4,4,5,5-테트라메틸-1,3,2-디옥사보롤란-2-일)벤조에이트

관련 CAS 번호: 178820-38-7 1190312-22-1 10406-24-3 147000-09-7 124909-04-2 17315-76-3 106824-96-8 144606-96-2 15398-91-1 159847-71-9

표준명의 마케팅 및 가격
제조업체 및 유통업체:
  • 제조/브랜드
  • 화학물질 및 원자재
  • 포장
  • 가격
  • AK Scientific
  • 3-Hydroxy-4-methoxycarbonylphenylboronic acid pinacol ester
  • 1g
  • $ 264.00
  • Ambeed
  • Methyl2-hydroxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 98%
  • 100mg
  • $ 73.00
  • Ambeed
  • Methyl2-hydroxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 98%
  • 250mg
  • $ 96.00
  • Ambeed
  • Methyl2-hydroxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 98%
  • 1g
  • $ 218.00
  • Ambeed
  • Methyl2-hydroxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 98%
  • 5g
  • $ 751.00
  • American Custom Chemicals Corporation
  • 3-HYDROXY-4-METHOXYCARBONYLPHENYLBORONIC ACID PINACOL ESTER 95.00%
  • 1G
  • $ 397.69
  • Chemenu
  • Methyl2-hydroxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 98%
  • 5g
  • $ 498.00
  • Chemenu
  • Methyl2-hydroxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 98%
  • 1g
  • $ 148.00
  • Crysdot
  • Methyl2-hydroxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 95+%
  • 1g
  • $ 238.00
  • Matrix Scientific
  • Methyl 2-hydroxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 95+%
  • 250mg
  • $ 243.00
총 17 개 원재료 공급업체
표준명의 화학적 성질 Edit
물리적 데이터:
안전정보:
  • 픽토그램: Xn
  • 위험 코드: Xn
  • 진술: 22
  • 안전 선언문:
사용:
  • 소개 및 적용: 3-Hydroxy-4-methoxycarbonylphenylboronic acid, pinacol ester is a chemical compound that is used in organic synthesis. It is a boronic acid derivative that has a protective pinacol ester group, which can be removed under certain conditions to reveal the boronic acid functionality. This compound is commonly used in Suzuki-Miyaura cross-coupling reactions, which are used to form carbon-carbon bonds between an aryl or vinyl halide and an organoboron compound. The pinacol ester group protects the boronic acid during the reaction, and can be removed after the reaction is complete to yield the desired product. This compound is also used in other types of organic reactions, such as Heck reactions and Stille reactions, to form carbon-carbon bonds. It is a versatile reagent that can be used in a variety of synthetic applications.
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