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1236254-73-1

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1236254-73-1 Usage

Drug Class

Diuretic

Primary Use

Treatment of high blood pressure and fluid retention

Mechanism of Action

Increases urine production to decrease fluid buildup in the body

Administration

Orally as a tablet or liquid

Dosage

To be determined by healthcare professional

Side Effects

Dizziness, lightheadedness, dehydration

Severe Side Effects

Require immediate medical attention

Interactions

Potential interactions with other medications

Importance

Valuable in managing high blood pressure and fluid retention caused by various conditions

Check Digit Verification of cas no

The CAS Registry Mumber 1236254-73-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,6,2,5 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1236254-73:
(9*1)+(8*2)+(7*3)+(6*6)+(5*2)+(4*5)+(3*4)+(2*7)+(1*3)=141
141 % 10 = 1
So 1236254-73-1 is a valid CAS Registry Number.

1236254-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-N-cyclohexyl-3-methylbutanamide hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:1236254-73-1 SDS

1236254-73-1Downstream Products

1236254-73-1Relevant articles and documents

Development of new catalytic enantioselective formation of methylenelactam-based N,O-spirocyclic compounds via ring opening-asymmetric reclosure of hydroxylactams

Sengoku, Tetsuya,Miyoshi, Ayako,Tsuda, Tamaki,Inuzuka, Toshiyasu,Sakamoto, Masami,Takahashi, Masaki,Yoda, Hidemi

, (2020/05/18)

Catalytic enantioselective formation of methylenelactam-based N,O-spirocyclic compounds is developed. Hydroxylactams prepared from N-carbonyl phthalimides and β-amido functionalized allylboronates underwent ring opening-asymmetric reclosure in the presence of catalytic amounts of MgBr2 and a chiral aminophenol to afford the corresponding N,O-spirocyclic compounds in excellent yields and high enantioselectivities.

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