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1,2-Propanediol, 3-[(1,1-dimethylethyl)amino]-, 1-(4-aminobenzoate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90531-56-9

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90531-56-9 Usage

Functional Groups

Hydroxyl groups (-OH) in 1,2-position, amino group ((-NH2) in 3-position), and a 4-aminobenzoate group (-NH-C6H4-COO-)

Molecular Structure

A propane backbone with two hydroxyl groups and an amino group attached to the 3rd carbon, and a 4-aminobenzoate group attached to the 1st carbon

Usage in Industries

Pharmaceutical, cosmetics, skincare, and hair care products

Properties

Moisturizing, skin-conditioning, solvent, and viscosity decreasing agent

Applications

Skincare products, creams, lotions, hair care products, and over-the-counter medications

Versatility

Wide range of applications and multiple uses in different industries

Check Digit Verification of cas no

The CAS Registry Mumber 90531-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,3 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90531-56:
(7*9)+(6*0)+(5*5)+(4*3)+(3*1)+(2*5)+(1*6)=119
119 % 10 = 9
So 90531-56-9 is a valid CAS Registry Number.

90531-56-9Downstream Products

90531-56-9Relevant academic research and scientific papers

propanolamines. 1. Novel β-Blockers with Ultrashort Duration of Action

Kam, Sheung-Tsam,Matier, William L.,Mai, Khuong X.,Barcelon-Yang, Cynthia,Borgman, Robert J.,et al.

, p. 1007 - 1016 (2007/10/02)

Novel propanolamines were synthesized and investigated as potential ultrashort-acting β-adrenergic receptor blockers.Many of these analogues exhibited good potency and short duration.The N-ureidoalkyl analogue 85 (ACC-9089) has a potency equal to propranolol and a duration of action of about 21 min in the dog.It has been selected as a candidate for further clinical study.Structure-activity relationships and structure-duration relationships for these new β-blockers are also discussed.

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