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产品详情
产品名称 英文名称:4-Iodophenylboronic acid MIDA ester(contains varying amounts of Anhydride) 同义词 2-(4-Iodophenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione、1257649-56-1、4-Iodophenylboronic acid MIDA ester、1287221-36-6、DTXSID20746271、MFCD11215234、AKOS022168234、AS-2788、4-Iodophenylboronic acid MIDA ester, 97%、CS-0443792、A910538、2-(4-碘苯基)-6-甲基-1,3,6,2-二氧氮杂硼烷-4,8-二酮(含有数量不等的酸酐) 产品性质 CAS编号:1257649-56-1 分子式:C11H11BINO4 分子量:358.92 MDL号:MFCD11215234 PubChem编号:71310644 别名:2-(4-碘苯基)-6-甲基-1,3,6,2-二氧氮杂硼烷-4,8-二酮(含有数量不等的酸酐) 英文别名:2-(4-Iodophenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione|1257649-56-1|4-Iodophenylboronic acid MIDA ester|1287221-36-6|DTXSID20746271|MFCD11215234|AKOS022168234|AS-2788|4-Iodophenylboronic acid MIDA ester, 97%|CS-0443792|A910538 规格或纯度:97% 英文名称:4-Iodophenylboronic acid MIDA ester(contains varying amounts of Anhydride) 储存温度:2-8°C储存 运输条件:冰袋运输 产品介绍:Product ApplicationSuzuki Cross-Coupling with MIDA Boronates4-Iodophenylboronic acid MIDA ester can be usedAs a starting material to prepare rod-like hydrogen-bonded organic frameworks through Stille-coupling using 2,5-bis(trimethyltin)heterocycle, Pd(PPh3)4, and CuI. As a substrate in the C-H arylation reaction of pyroglutamic acid derivatives with aryl and heteroaryl iodides; catalyzed by the palladium catalyst. As a substrate in the synthesis of trifluoroborates, which are further converted to protected boronic acids. As a starting material in the synthesis of amino acid MIDA boronates as new building blocks by reacting with protected iodoalanine. IUPAC Name:2-(4-iodophenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione INCHI:InChI=1S/C11H11BINO4/c1-14-6-10(15)17-12(18-11(16)7-14)8-2-4-9(13)5-3-8/h2-5H,6-7H2,1H3 InChi Key:KIKNJEGAWBNFLW-UHFFFAOYSA-N Canonical SMILES:B1(OC(=O)CN(CC(=O)O1)C)C2=CC=C(C=C2)I Isomeric SMILES:B1(OC(=O)CN(CC(=O)O1)C)C2=CC=C(C=C2)I WGK Germany:3 PubChem CID:71310644 熔点:213-217 °C 象形图: 信号词:Warning 危险声明:H302 Harmful if swallowed 预防措施声明:P501,P264,P270,P330,P301+P317 个人防护装备:dust mask type N95 (US), Eyeshields, Gloves 产品包装
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