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1195967-46-4

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1195967-46-4 Usage

General Description

(R)-2-amino-2-methyl-dec-6-enoic acid, also known as Leucic acid, is an α-amino acid with the chemical formula C11H21NO2. It is a naturally occurring compound found in certain foods such as beef, fish, and dairy products. Leucic acid is known for its potential benefits in promoting muscle protein synthesis and muscle growth, making it a popular supplement in the fitness and bodybuilding industry. It is also believed to have anti-catabolic effects, helping to prevent muscle breakdown and improve recovery after exercise. Additionally, leucic acid has been studied for its potential role in improving insulin sensitivity and fat metabolism, making it of interest for those looking to improve their body composition and overall health.

Check Digit Verification of cas no

The CAS Registry Mumber 1195967-46-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,5,9,6 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1195967-46:
(9*1)+(8*1)+(7*9)+(6*5)+(5*9)+(4*6)+(3*7)+(2*4)+(1*6)=214
214 % 10 = 4
So 1195967-46-4 is a valid CAS Registry Number.

1195967-46-4SDS

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 2-amino-2-methyldec-6-enoic 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

Emergency phone number -
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More Details:1195967-46-4 SDS

1195967-46-4Upstream product

1195967-46-4Relevant articles and documents

Robust asymmetric synthesis of unnatural alkenyl amino acids for conformationally constrained α-helix peptides

Aillard, Boris,Robertson, Naomi S.,Baldwin, Adam R.,Robins, Siobhan,Jamieson, Andrew G.

supporting information, p. 8775 - 8782 (2014/12/11)

The efficient asymmetric synthesis of unnatural alkenyl amino acids required for peptide 'stapling' has been achieved using alkylation of a fluorine-modified NiII Schiff base complex as the key step.

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