Home Cart Sign in  
Chemical Structure| 652-37-9 Chemical Structure| 652-37-9
Chemical Structure| 652-37-9

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

Acefylline is an adenosine receptor antagonist, a stimulant drug of the xanthine chemical class.

Synonyms: Acefylline; Theophyllineacetic acid; NSC 52996

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 Theophylline-7-acetic Acid

CAS No. :652-37-9
Formula : C9H10N4O4
M.W : 238.20
SMILES Code : CN1C2=C(N(CC(O)=O)C=N2)C(=O)N(C)C1=O
Synonyms :
Acefylline; Theophyllineacetic acid; NSC 52996
MDL No. :MFCD00022832
InChI Key :HCYFGRCYSCXKNQ-UHFFFAOYSA-N
Pubchem ID :69550

Safety of Theophylline-7-acetic Acid

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501

Application In Synthesis of Theophylline-7-acetic 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 [ 652-37-9 ]

[ 652-37-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 652-37-9 ]
  • [ 3575-32-4 ]
  • [ 1243259-28-0 ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20℃; for 2h; To a solution of acid in DMF were added HATU5 DIEA, and aniline in that order. The reaction mixture was stirred for 2hr at room temperature. [00316] After the reaction was complete (LC-MS and TLC)5 the compound was purified by prep-HPLC (250mg). Compound 24 was characterized by 1H NMR5 LC-MS and HPLC. 1H NMR (CDC13), delta: 9.25 (s, IH), 7.77 (s5 IH), 7.15 (t, J=8.14 Hz5 IH)5 7.05 (s, IH)5 6.74-6.80 (m, IH)5 6.46-6.53 (m5 IH), 4.95 (s5 2H)5 3.61 (s, 3H), 3.46 (s, 3H), 2.93 (s, 6H)5 1.59 (s, 3H). LC-MS5 (M+l), 357. HPLC (>;95%, retention time, 5.79 min).
 

Historical Records

Categories