Dihydroxyfumaric acid dihydrate

Names

[ CAS No. ]:
20688-70-4

[ Name ]:
Dihydroxyfumaric acid dihydrate

[Synonym ]:
dihydroxy-fumaric acid,dihydrate
Difenyl-dihydroxysilan
dihydroxydiphenylsilane
Dihydroxy-fumarsaeure,Dihydrat
diphenylsilane
Silanediol,diphenyl
diphenyl-silanedio
Diphenylsilandiol

Chemical & Physical Properties

[ Melting Point ]:
-155ºC (dec.)

[ Molecular Formula ]:
C₄H₈O₈

[ Molecular Weight ]:
184.10200

[ Exact Mass ]:
184.02200

[ PSA ]:
133.52000

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2918199090

Customs

[ HS Code ]: 2918199090

[ Summary ]:
2918199090 other carboxylic acids with alcohol function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Exploratory experiments on the chemistry of the "glyoxylate scenario": formation of ketosugars from dihydroxyfumarate.

J. Am. Chem. Soc. 134(7) , 3577-89, (2012)

In the context of a "glyoxylate scenario" of primordial metabolism, the reactions of dihydroxyfumarate (DHF) with reactive small molecule aldehydes (e.g., glyoxylate, formaldehyde, glycolaldehyde, and...

Production of tartrates by cyanide-mediated dimerization of glyoxylate: a potential abiotic pathway to the citric acid cycle.

J. Am. Chem. Soc. 135(36) , 13440-5, (2013)

An abiotic formation of meso- and DL-tartrates in 80% yield via the cyanide-catalyzed dimerization of glyoxylate under alkaline conditions is demonstrated. A detailed mechanism for this conversion is ...

The preparation and properties of lithium hydroxypyruvate and hydroxypyruvic acid.

Biochem. J. 68(1) , 74-81, (1958)

dihydroxyfumaric acid
Dihydroxyfumaric acid (hydrate)
RHODIZONIC ACID DIHYDRATE
oxalic acid,dihydrate
nitric acid,dihydrate
carbonic acid,dihydrate
6-methyl-2-((1-(2-phenylacetyl)piperidin-4-yl)methyl)pyridazin-3(2H)-one
2-((1-(2-(4-fluorophenyl)acetyl)piperidin-4-yl)methyl)-6-methylpyridazin-3(2H)-one
2-((1-(3-methoxybenzoyl)piperidin-4-yl)methyl)-6-methylpyridazin-3(2H)-one
2-((1-(4-methoxybenzoyl)piperidin-4-yl)methyl)-6-methylpyridazin-3(2H)-one
2-((1-(4-(dimethylamino)benzoyl)piperidin-4-yl)methyl)-6-methylpyridazin-3(2H)-one
2-(2-Fluorophenoxy)-1-{3-[(oxolan-3-yl)methoxy]azetidin-1-yl}propan-1-one
N-[(6-cyclopropylpyridin-3-yl)methyl]-6-ethoxypyridine-3-carboxamide
N-((6-cyclopropylpyridin-3-yl)methyl)-4-morpholinobenzamide
2-(4-(((6-Cyclopropylpyrimidin-4-yl)oxy)methyl)piperidin-1-yl)-4-methoxypyrimidine
4-(3-methoxypyrrolidin-1-yl)-N-(4-methylphenyl)piperidine-1-carboxamide

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