168017
meso-2,3-Dimethylsuccinic acid
99%
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About This Item
Linear Formula:
HO2CCH(CH3)CH(CH3)CO2H
CAS Number:
Molecular Weight:
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
Related Categories
Application
meso-2,3-Dimethylsuccinic acid was used in the synthesis of:
- meso-1,4-diiodo-2,3-dimethylbutane
- selenoacetal with an erythro-configured CHMe-CHMe fragment
- erythro-4-acetoxy-2,3-dimethylbutan-1-ol
- (±)-faranal
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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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