Diphenylacetic acid

Catalog No.: A86921
Biochemical Reagent
Diphenylacetic acid is a biochemical reagent primarily known for its role in asymmetric synthesis. It facilitates the kinetic resolution of racemic 2-hydroxy-γ-butyrolactones through asymmetric esterification, utilizing pivalic anhydride and a chiral acyl-transfer catalyst. Additionally, it serves as a catalyst in the synthesis of 2-allyl-3-oxazolin-5-one derivatives via Rh-catalyzed coupling reactions of azlactones with alkynes, followed by aza-Cope rearrangement. Its applications are valuable in organic synthesis and pharmaceutical research.
Grouped product items
Size Price Stock Qty
1mg
$20.00
In stock
5g
$25.00
In stock
25g
$30.00
In stock
50g
$35.00
In stock
100g
$40.00
In stock
500g
$85.00
In stock
Bulk Size
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Free Delivery on orders over $500
Research use only. We do not sell to patients.

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionDiphenylacetic acid is a biochemical reagent primarily known for its role in asymmetric synthesis. It facilitates the kinetic resolution of racemic 2-hydroxy-γ-butyrolactones through asymmetric esterification, utilizing pivalic anhydride and a chiral acyl-transfer catalyst. Additionally, it serves as a catalyst in the synthesis of 2-allyl-3-oxazolin-5-one derivatives via Rh-catalyzed coupling reactions of azlactones with alkynes, followed by aza-Cope rearrangement. Its applications are valuable in organic synthesis and pharmaceutical research.
Product Information
Catalog NumA86921
FormulaC14H12O2
Molecular Weight212.25
CAS Number117-34-0
SMILESO=C(O)C(C1=CC=CC=C1)C2=CC=CC=C2
SynonymsDiphenylmethane-α-carboxylic Acid
Useful Calculator

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Mass (mg) = Concentration (mM) × Volume (mL) × Molecular Weight (g/mol)

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This equation is commonly abbreviated as: C1V1 = C2V2

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