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Acetyl chloride, amino-(9CI), also known as aminoacetyl chloride, is a chemical compound with the molecular formula C2H4ClNO. It is an acyl chloride, which means it contains a functional group derived from carboxylic acids. Acetyl chloride, amino-(9CI) is characterized by its pungent odor and high reactivity, making it potentially hazardous to handle. It is used in various chemical reactions as an acetylating agent, particularly in the synthesis of pharmaceuticals and other organic compounds.

4746-64-9

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4746-64-9 Usage

Uses

Used in Pharmaceutical Industry:
Acetyl chloride, amino-(9CI) is used as an acetylating agent for the synthesis of various pharmaceuticals. Its reactivity allows it to readily form acetylated products, which are essential in the production of certain drugs and medications.
Used in Organic Synthesis:
In the field of organic chemistry, Acetyl chloride, amino-(9CI) is utilized as an acetylating agent for the synthesis of various organic compounds. Its ability to form acetylated products makes it a valuable reagent in the preparation of different organic molecules.
Due to the high reactivity of Acetyl chloride, amino-(9CI), it can react violently with water and other compounds containing hydroxyl groups. It is essential to handle Acetyl chloride, amino-(9CI) with extreme caution and use it in a well-ventilated environment by trained professionals to minimize the risk of irritation to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 4746-64-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,4 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4746-64:
(6*4)+(5*7)+(4*4)+(3*6)+(2*6)+(1*4)=109
109 % 10 = 9
So 4746-64-9 is a valid CAS Registry Number.

4746-64-9SDS

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 glycyl chloride

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:4746-64-9 SDS

4746-64-9Relevant academic research and scientific papers

NOVEL CONJUGATES, PHARMACEUTICAL COMPOSITIONS INCLUDING SAME AND USES THEREOF

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Page/Page column 39, (2008/06/13)

Novel conjugates of a gamma-aminobutyric acid (GABA) compound or a glycine compound and an analgesic drug are disclosed. Further disclosed are pharmaceutical compositions containing these conjugates and uses thereof in the treatment of CNS-associated diseases or disorders.

Influence of solvent viscosity on the rate of hydrolysis of dipeptides by carboxypeptidase Y

Kanosue, Yoshifumi,Kojima, Satoshi,Ohkata, Katsuo

, p. 448 - 457 (2007/10/03)

The influence of solvent viscosity on the rate of enzymatic hydrolysis of a series of dipeptides (Z-Phe-Gly, Z-Phe-Sar, Z-Phe-Ala, Z-Phe-NMeAla, Z-Phe-Aib and Z-Phe-Pro) by carboxypeptidase Y was investigated. The effect of solvent viscosity on the enzymatic hydrolysis revealed that whereas all Kcat values decreased with viscosity, those of the N-alkyl peptides decreased more than those of the N-H peptides. The kinetic behaviour implies the involvement of conformational changes of the enzyme in terms of the 'induced-fit' process. Copyright

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