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方案
96%
mp
131-134 °C (lit.)
官能团
aldehyde
SMILES字符串
COc1cc(C=O)cc(O)c1O
InChI
1S/C8H8O4/c1-12-7-3-5(4-9)2-6(10)8(7)11/h2-4,10-11H,1H3
InChI key
RRKMWVISRMWBAL-UHFFFAOYSA-N
相关类别
一般描述
3,4-Dihydroxy-5-methoxybenzaldehyde can be obtained by reactting 5-iodovaniliin with sodium hydroxide and copper sulfate solution.
应用
3,4-Dihydroxy-5-methoxybenzaldehyde may be used for the preparation of 3,4-dihydroxy-6-methoxy-β-nitrostyrene and 5-hydroxyconiferyl alcohol.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Structure and synthesis of (?)-Wuweizisu C.
Schneiders GE and Stevenson R.
The Journal of Organic Chemistry, 46(41), 2969-2971 (1981)
Thomas Goujon et al.
Plant molecular biology, 51(6), 973-989 (2003-06-05)
A promoter-trap screen allowed us to identify an Arabidopsis line expressing GUS in the root vascular tissues. T-DNA border sequencing showed that the line was mutated in the caffeic acid O-methyltransferase 1 gene (AtOMT1) and therefore deficient in OMT1 activity.
MESCALINE ANALOGS. III. 2, 4, 6-TRIALKYL-AND 3, 4-DIHYDROXY-5-METHOXY-?-PHENETHYLAMINES.
Benington F, et al.
The Journal of Organic Chemistry, 20(9), 1292-1296 (1955)
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