CAS: 37443-42-8; Methyl Tetrahydrofuran-2-Carboxylate

相似化合物

22415-59-4 97-99-4 87392-07-2

上下游产品

CAS号611-13-2 2-糠酸甲酯 | CAS号16874-33-2 2-四氢呋喃甲酸 | CAS号67-56-1 甲醇 | CAS号52449-98-6 四氢呋喃-2-甲酰氯 | CAS号87324-01-4 (S)-TETRAHYDROF... | CAS号87392-07-2 (S)-(-)-四氢呋喃-2-羧酸 | CAS号87392-05-0 (R)-(+)-四氢呋喃-2-甲酸 | CAS号87324-00-3 (R)-TETRAHYDROF... | CAS号81403-67-0 N-(3-甲胺基丙基)四氢呋喃... | CAS号63074-07-7 1-(四氢-2-糠酰)哌嗪 | CAS号1191-99-7 2,3-二氢呋喃 | CAS号1708-29-8 2,5-二氢呋喃 | CAS号67-56-1 甲醇 | CAS号1489-69-6 环丙甲醛

2-四氢呋喃甲酸置于氯化亚砜体系中,化学反应生成2-四氢糠酸甲酯
参考文献:环氧乙烷-2-基-羧酸,环氧乙烷-2-基-甲醇和环氧烷-2-基-甲醇衍生的几种酯的电化学氟化
标题:环氧乙烷-2-基-羧酸,环氧乙烷-2-基-甲醇和环氧烷-2-基-甲醇衍生的几种酯的电化学氟化
摘要:研究了环氧乙烷-2-基-羧酸(1),环氧乙烷-2-基-甲醇(2)和环氧烷-2-基-甲醇(3)的酯衍生物的电化学氟化(ecf).全氟(氧杂环戊烷-2-基-Carbonylfluoride)(4)从的衍生物获得的1和2,和全氟(氧杂环己烷-2-基-Carbonylfluoride)(5从衍生物获得)3作为所需化合物,分别.从2和3的乙酸盐的ecf,还以低收率获得了具有二氧戊环环的全氟螺醚与所需的全氟酰氟(4和5).通过分析通过与alcl 3反应获得的氯化产物,证实了这些全氟螺醚的结构.
Doi:10.1016/j.Jfluchem.2004.11.014

专利信息

专利号:US-7335502-B2
优先权日:2002-10-07
标题:Chlorohydrin and hydroxycarboxylic ester asymmetric hydrolase gene
发明人：NAKAGAWA ATSUSHI; SUZUKI TOSHIO; SHINMYO ATSUHIKO; KATO KO; IDOGAKI HIDEAKI
权利人:DAISO CO LTD
摘要:The present invention is to provide a gene having asymmetric hydrolase activity which is useful for synthesis of an optically active carboxylic acid, its antipode ester, and lactone, and a hydroxycarboxylic ester asymmetric hydrolase enzyme (EnHCH) derived from Enterobacter sp. DS-S-75 strain (FERM BP-5494) which is bacteria belonging to the genus Enterobacter , a EnHCH gene shown by base sequence of SEQ. ID. NO: 1, a gene encoding a protein having an amino acid sequence of SEQ. ID. NO: 2, and E. coli DH5α (pKK-EnHCH) deposited to International Patent Organism Depositary, National Institute of Advanced Industrial Science and Technology as a deposition No. FERM BP-08466.

专利号:US-2008200475-A1
优先权日:2005-03-28
标题:4-Piperazinothieno[2,3-D] Pyrimidine Compounds As Platelet Aggregation Inhibitors
发明人：ENNIS MICHAEL DALTON; KORTUM STEVEN WADE; TENBRINK RUTH ELIZABETH
权利人:PFIZER
摘要:Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula I: (I) wherein A 1 , A 2 , A 3 , A 4 , A 5 , A 6 , A 7 , A 8 , X 4 , X 6 , R 2a , R x , R 4 , R 5 , and R 6 are as defined in the detailed description of the invention. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

专利号:US-2024049711-A1
优先权日:2020-12-24
标题 :Herbicide composition and weed controlling method
发明人：OKAJIMA YUKI; TORIUMI MAI; SADA YOSHINAO
权利人:SUMITOMO CHEMICAL CO
摘要:A herbicidal composition including one or more uracil compounds selected from the group consisting of a compound of formula (I):a compound of formula (II):and a compound of formula (III):and one or more compounds selected from the group consisting of the herbicide compound group B and the safener group C, wherein the herbicide compound group B is the group consisting of the following B-1 to B-12: B-1, acetolactate synthase inhibitors; B-2, acetyl CoA carboxylase inhibitors; B-3, protoporphyrinogen IX oxidase inhibitors; B-4, 4-hydrophenylpyrubic acid dioxygenase inhibitors; B-5, phytoene desaturase inhibitors; B-6, photosystem II inhibitors; B-7, very-long-chain fatty acid synthesis inhibitors; B-8, microtubule formation inhibitors; B-9, auxin-type herbicides; B-10, enolpyruvylshikimate-3-phosphate synthase inhibitors; B-11, glutamine synthase inhibitors; and B-12, other herbicides; (including agriculturally acceptable salts or derivatives thereof).

专利号:KR-20140041380-A
优先权日:2010-09-20
标题 :Synthesis method of beta-dicarbonyl compound