Home Cart Sign in  
Chemical Structure| 42013-20-7 Chemical Structure| 42013-20-7
Chemical Structure| 42013-20-7

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

2-(2-Methylbenzamido)acetic acid is a metabolite detected in urine.

Synonyms: o-Toluric Acid; NSC 163983; 2-MHA

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of 2-Methylhippuric Acid

CAS No. :42013-20-7
Formula : C10H11NO3
M.W : 193.20
SMILES Code : O=C(O)CNC(C1=CC=CC=C1C)=O
Synonyms :
o-Toluric Acid; NSC 163983; 2-MHA
MDL No. :MFCD00050991
InChI Key :YOEBAVRJHRCKRE-UHFFFAOYSA-N
Pubchem ID :91637

Safety of 2-Methylhippuric Acid

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 2-Methylhippuric Acid

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 42013-20-7 ]

[ 42013-20-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 42013-20-7 ]
  • [ 34595-26-1 ]
  • [ 1447964-05-7 ]
YieldReaction ConditionsOperation in experiment
31% With sodium acetate; acetic anhydride; In neat (no solvent); at 95℃; General procedure: A mixture of <strong>[34595-26-1]2-(piperidin-1-yl)benzaldehyde</strong> (0.946 g, 5 mmol) and 2-benzamidoacetic acid (0.896 g, 5 mmol) was heated in 95 C with the addition of NaOAc (2.5 mmol) and Ac2O (5 mmol). After completion of the reaction, 2 mL ethanol was added to the mixture and was stirred for 10 h at room temperature. The solid was filtered off, washed with water, and ice-cold ethanol. The crude product was recrystallized from toluene to give the corresponding (Z)-alkylidene azlactones 1a (Note: For the preparation of compounds 1b-n, the corresponding crude products were recrystallized from ethanol to give the desired products 1b-n).
  • 2
  • [ 42013-20-7 ]
  • [ 34595-26-1 ]
  • 2-o-tolyl-1',2',3',4',4a',6'-hexahydro-5H-spiro[oxazole-4,5'-pyrido[1,2-a]quinolin]-5-one [ No CAS ]
  • 2-o-tolyl-1',2',3',4',4a',6'-hexahydro-5H-spiro[oxazole-4,5'-pyrido[1,2-a]quinolin]-5-one [ No CAS ]
 

Historical Records

Technical Information

Categories