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Pentanoic acid, 5-(phenylamino)-, also known as 5-phenylpentanoic acid or phenylalanine, is an organic compound with the chemical formula C11H15NO2. It is a non-essential amino acid, meaning that it can be synthesized by the human body, and is one of the 20 standard amino acids used to build proteins. Phenylalanine plays a crucial role in various physiological processes, including the synthesis of neurotransmitters, such as dopamine, norepinephrine, and epinephrine, and the production of melanin, a pigment responsible for skin, hair, and eye color. It is also involved in the regulation of appetite and mood. Phenylalanine is found in various protein-rich foods, such as meat, fish, eggs, and dairy products, and is commercially produced through the fermentation of carbohydrates or the hydrolysis of proteins.

7707-01-9

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7707-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7707-01-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,0 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7707-01:
(6*7)+(5*7)+(4*0)+(3*7)+(2*0)+(1*1)=99
99 % 10 = 9
So 7707-01-9 is a valid CAS Registry Number.

7707-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(phenylamino)pentanoic acid

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

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More Details:7707-01-9 SDS

7707-01-9Downstream Products

7707-01-9Relevant academic research and scientific papers

Novel hydroxyphenylurea dual inhibitor against Acyl-CoA: Cholesterol acyltransferase (ACAT) and low density lipoprotein (LDL) oxidation as antiatherosclerotic agent

Nakao, Kazuya,Kubota, Hitoshi,Yasuhara, Mikiko,Saito, Keiko,Suzuki, Toshikazu,Ohmizu, Hiroshi,Shimizu, Ryo

, p. 853 - 861 (2007/10/03)

Novel hydroxyphenylurea derivatives were synthesized and their inhibitory potency evaluated against acyl-CoA: cholesterol acyltransferase ACAT. Quantitative structure-activity relationship analysis revealed that their ACAT inhibitory activities were controlled by the hydrophobicity of the whole molecule, the substitution pattern of urea moiety, and the existence of carboxylic acid. The derivatives with strong activities inhibited foam cell formations. Moreover, these compounds showed antioxidative effects against low density lipoprotein LDL, owing to their characteristic 3-tert-butyl-2-hydroxy-5-methoxyphenyl substructure. Based on the mechanism of atherosclerosis generation, this hydroxyphenylurea-type dual inhibitor against both ACAT and LDL oxidation is expected to be a promising drug for atherosclerosis. Copyright

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