168017
内消旋-2,3-二甲基琥珀酸
99%
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关于此项目
线性分子式:
HO2CCH(CH3)CH(CH3)CO2H
化学文摘社编号:
分子量:
146.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
210-163-1
MDL number:
Assay:
99%
Form:
powder
InChI key
KLZYRCVPDWTZLH-ZXZARUISSA-N
InChI
1S/C6H10O4/c1-3(5(7)8)4(2)6(9)10/h3-4H,1-2H3,(H,7,8)(H,9,10)/t3-,4+
SMILES string
C[C@@H]([C@@H](C)C(O)=O)C(O)=O
assay
99%
form
powder
mp
200 °C (dec.) (lit.)
functional group
carboxylic acid
Quality Level
Application
内消旋-2,3-二甲基琥珀酸被用于合成：
- 内消旋-1,4-二碘-2,3-二甲基丁烷
- 硒缩醛，具有赤型配置的CHMe-CHMe片段
- 赤型-4-乙酰氧基-2,3-二甲基丁-1-醇
- (±)-faranal
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Highly selective formation of eight-membered-ring systems by oxidative cyclization with molybdenum pentachloride-an environmentally friendly and inexpensive access to 2,2'-cyclolignans.
Beate Kramer et al.
Angewandte Chemie (International ed. in English), 41(16), 2981-2982 (2002-08-31)
Synthesis of (3S*, 4R*, 6E, 10Z)-3, 4, 7, 11-tetramethyltrideca-6, 10-dienal (faranal) using stereospecific 1, 4-cis-hydrogenation of conjugated double bonds.
Vasil'ev AA, et al.
Journal of the Chemical Society. Perkin Transactions 1, 14, 2211-2216 (2000)
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