CAS 15042-01-0

(+)-5,6-O-isopropylidène-L-ascorbique acide

Formule : C₉H₁₂O₆

InChI : InChI=1/C9H12O6/c1-9(2)13-3-4(15-9)7-5(10)6(11)8(12)14-7/h4,7,10-11H,3H2,1-2H3/t4-,7+/m0/s1

Code InChI : POXUQBFHDHCZAD-MHTLYPKNSA-N

SMILES : CC1(OC[C@H](O1)[C@@H]2C(=C(C(=O)O2)O)O)C

Synonymes :

• Ascorbic Acid Acetonide
• 5,6-O-(1-methylethylidene)hex-1-enofuranos-3-ulose
• (2R)-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-4,5-dihydroxy-furan-3-one
• (5R)-5-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3,4-dihydroxyfuran-2(5H)-one (non-preferred name)
• L-Ascorbic Acid Acetonide
• (+)-5,6-O-Isopropylidene-L-Ascorbic Acid

(+)-5,6-O-Isopropylidene-L-ascorbic Acid

CAS : 15042-01-0

Formule : C₉H₁₂O₆

Degré de pureté : >98.0%(HPLC)(T)

Couleur et forme : White to Almost white powder to crystal

Masse moléculaire : 216.19

Ref: 3B-I0507

(+)-5,6-O-Isopropylidene-L-ascorbic acid

CAS : 15042-01-0

(+)-5,6-O-Isopropylidene-L-ascorbic acid

Formule : C₉H₁₂O₆

Degré de pureté : >98%

Couleur et forme : Solid-Powder

Masse moléculaire : 216.18798

Ref: 54-OR7870T

Ascorbic acid acetonide

CAS : 15042-01-0

Masse moléculaire : 216.19

Ref: 7W-GC3676

(R)-5-((S)-2,2-Dimethyl-1,3-dioxolan-4-yl)-3,4-dihydroxyfuran-2(5H)-one

CAS : 15042-01-0

Formule : C₉H₁₂O₆

Degré de pureté : 95%

Couleur et forme : Solid

Masse moléculaire : 216.1880

Ref: IN-DA001MLK

Ascorbic Acid Acetonide

Produit contrôlé

CAS : 15042-01-0

Applications Ascorbic Acid Acetonide (cas# 15042-01-0) is a compound useful in organic synthesis.
References Shibayama, H., et al.: Biosci., Biotechnol., Biochem., 72, 1015 (2008), Choi, H., et al.: Bioorg. Med. Chem. Lett., 19, 2079 (2009),

Formule : C₉H₁₂O₆

Couleur et forme : Neat

Masse moléculaire : 216.19

Ref: TR-A787000

5,6-O-Isopropylidene-L-ascorbic acid

CAS : 15042-01-0

(R)-5-((S)-2,2-Dimethyl-1,3-dioxolan-4-yl)-3,4-dihydroxyfuran-2(5H)-one

Formule : C₉H₁₂O₆

Degré de pureté : 95%

Masse moléculaire : 216.19

Ref: IN-DG11358

5,6-O-Isopropylidene-L-ascorbic acid

CAS : 15042-01-0

5,6-O-Isopropylidene-L-ascorbic acid is an access to the vitamin C molecule. It can be synthesized from L-ascorbic acid by reacting with isopropyl iodide and hydrochloric acid. Cryo-electron microscopy has been used to identify the location of 5,6-O-Isopropylidene-L-ascorbic acid in human ganglion cells. This compound has a number of physiological activities and is one of the most powerful antioxidants found in humans. 5,6-O-Isopropylidene-L-ascorbic acid is a precursor to retinoic acid and hydrogen chloride, which are important for erythropoietin production in the kidneys. Dehydroascorbate (DHA) is formed when 5,6-O-Isopropylidene-L-ascorbic acid reacts with hydrogen chloride. D

Formule : C₉H₁₂O₆

Degré de pureté : Min. 95%

Masse moléculaire : 216.19 g/mol

Ref: 3D-MI03487

(R)-5-((S)-2,2-Dimethyl-1,3-dioxolan-4-yl)-3,4-dihydroxyfuran-2(5H)-one

CAS : 15042-01-0

Formule : C₉H₁₂O₆

Degré de pureté : 95%

Couleur et forme : Solid

Masse moléculaire : 216.189

Ref: 10-F324038