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56776-01-3

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56776-01-3 Usage

Uses

Hydrochloride salt of Tulobuterol a sympathomimetic drug used as a transdermal patch, increases normal diaphragm muscle strength. A β-adrenergic receptor agonist, related structurally to Terbutaline (T109750).

General Description

Standard for Supelco MIP SPE cartridges. For more information request Supelco Literature T407075, T706019, T706030, T706020

Check Digit Verification of cas no

The CAS Registry Mumber 56776-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,7,7 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56776-01:
(7*5)+(6*6)+(5*7)+(4*7)+(3*6)+(2*0)+(1*1)=153
153 % 10 = 3
So 56776-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H18ClNO.ClH/c1-12(2,3)14-8-11(15)9-6-4-5-7-10(9)13;/h4-7,11,14-15H,8H2,1-3H3;1H/t11-;/m0./s1

56776-01-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Detail
  • TCI America

  • (T2954)  Tulobuterol Hydrochloride  >98.0%(HPLC)(T)

  • 56776-01-3

  • 100mg

  • 690.00CNY

  • Detail
  • Sigma-Aldrich

  • (53541)  Tulobuterol hydrochloride  VETRANAL, analytical standard

  • 56776-01-3

  • 53541-10MG

  • 3,637.53CNY

  • Detail

56776-01-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(tert-Butylamino)-1-(2-chlorophenyl)ethanol hydrochloride

1.2 Other means of identification

Product number -
Other names 2-(tert-butylamino)-1-(2-chlorophenyl)ethanol,hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:56776-01-3 SDS

56776-01-3Downstream Products

56776-01-3Relevant articles and documents

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

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

, p. 390 - 394 (2020/04/27)

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.

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