Welcome to LookChem.com Sign In|Join Free
  • or
Tulobuterol hydrochloride is a medication belonging to the class of drugs known as beta-2 adrenergic agonists, which are commonly used to treat conditions such as asthma and chronic obstructive pulmonary disease (COPD). It works by relaxing the muscles in the airways, thereby reducing inflammation and widening the air passages to make breathing easier. As a hydrochloride salt, it is a water-soluble form of the drug, which can be administered through various routes, including oral or injectable forms. Tulobuterol hydrochloride is known for its bronchodilating effects, helping to alleviate symptoms such as shortness of breath, wheezing, and coughing. It is important to use this medication under the guidance of a healthcare professional, as it can have side effects and may interact with other medications.

73626-66-1

Post Buying Request

73626-66-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

73626-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73626-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,2 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73626-66:
(7*7)+(6*3)+(5*6)+(4*2)+(3*6)+(2*6)+(1*6)=141
141 % 10 = 1
So 73626-66-1 is a valid CAS Registry Number.

73626-66-1Downstream Products

73626-66-1Relevant academic research and scientific papers

Synthesis of the β2-Agonist Tulobuterol and Its Metabolite 4-Hydroxytulobuterol

Burdeinyi, M. L.,Glushkova, M. A.,Popkov, S. V.

, p. 390 - 394 (2020)

Abstract: Alternative methods have been developed for the synthesis of theβ2-agonist tulobuterol and its metabolite4-hydroxytulobuterol with a similar activity. The proposed procedures utilizeavailable reagents, and the key stage in the synthesis is the formation ofintermediate oxirane according to the Corey–Chaykovsky reaction, followed byopening of the oxirane ring by the action of excess tert-butylamine. In the synthesis of 4-hydroxytulobuterol, thehydroxy group was protected by benzylation, and the protecting group was removedin the final stage by hydrogenation over carbon-supported palladium.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 73626-66-1