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CAS

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4-phenylbutanoyl chloride, with the molecular formula C10H11ClO, is a colorless to light yellow liquid characterized by a pungent odor. It is a chemical compound that serves as a versatile intermediate in the synthesis of a variety of organic compounds, particularly in the pharmaceutical and agrochemical sectors. Its utility extends to the creation of pharmaceuticals, flavorings, and fragrances, as well as in the preparation of esters, amides, and other organic compounds through acylation reactions. Due to its corrosive nature and potential to cause irritation to the skin, eyes, and respiratory system, careful handling is advised.

464917-79-1

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464917-79-1 Usage

Uses

Used in Pharmaceutical Industry:
4-phenylbutanoyl chloride is used as a reagent for the synthesis of pharmaceuticals, playing a crucial role in the development of new drugs and medicinal compounds. Its ability to participate in acylation reactions makes it an indispensable component in the creation of complex organic molecules.
Used in Agrochemical Industry:
In the agrochemical sector, 4-phenylbutanoyl chloride is utilized as a precursor in the production of various agrochemicals, contributing to the development of pesticides, herbicides, and other crop protection agents.
Used in Flavor and Fragrance Industry:
4-phenylbutanoyl chloride is employed as an intermediate in the synthesis of flavorings and fragrances, enhancing the aromatic profiles of various consumer products.
Used in Organic Chemistry Research:
As a versatile chemical intermediate, 4-phenylbutanoyl chloride is used in research for the development of new organic compounds and the exploration of novel chemical reactions and mechanisms.

Check Digit Verification of cas no

The CAS Registry Mumber 464917-79-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,4,9,1 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 464917-79:
(8*4)+(7*6)+(6*4)+(5*9)+(4*1)+(3*7)+(2*7)+(1*9)=191
191 % 10 = 1
So 464917-79-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO/c11-10(12)8-4-7-9-5-2-1-3-6-9/h1-3,5-6H,4,7-8H2

464917-79-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl (Z)-3-aminobut-2-enoate

1.2 Other means of identification

Product number -
Other names benzyl 3-aminocrotonate

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:464917-79-1 SDS

464917-79-1Upstream product

464917-79-1Relevant articles and documents

NEW ANALOGS AS ANDROGEN RECEPTOR AND GLUCOCORTICOID RECEPTOR MODULATORS

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Paragraph 0295; 0296; 0308, (2019/05/16)

The present invention relates to novel dihydropyridine derivatives of formula (I): as modulators of nuclear receptors selected from androgen receptor and glucocorticoid receptor, to processes for their preparation, to pharmaceutical compositions comprising said compounds and to the use of said for manufacturing a medicament for the treatment of pathological conditions or diseases that can improve by modulation of androgen receptor and/or glucocorticoid receptor, selected from cancer, metastasizing cancers, benign prostate hyperplasia, polycystic ovary syndrome (PCOS), hair loss, hirsutism, acne, hypogonadism, muscle wasting diseases, cachexia, Cushing's syndrome, anti-psychotic drug induced weight gain, obesity, post-traumatic stress disorder and alcoholism.

Direct catalytic asymmetric synthesis of N-heterocycles from commodity acid chlorides by employing α,β-unsaturated acylammonium salts

Vellalath, Sreekumar,Van, Khoi N.,Romo, Daniel

supporting information, p. 13688 - 13693 (2014/01/06)

Taming the beast, asymmetrically: Modulation of the reactivity of acid chlorides, using cinchona alkaloid catalysts, results in chiral α,β-unsaturated acylammoniums, which react with nucleophiles enantioselectively to give pyrrolidinones, piperid-2-ones,

7,8-DIHYDRO-1,6-NAPHTHYDRIN-5(6H)-ONES AND RELATED BICYCLIC COMPOUNDS AS INHIBITORS OF DIPEPTIDYL PEPTIDASE IV AND METHODS

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Page/Page column 48-49, (2008/12/05)

The present application provides compounds, including all stereoisomers, solvates, prodrugs and pharmaceutically acceptable forms thereof according to Formula I. Additionally, the present application provides pharmaceutical compositions containing at leas

Pyrrolopyridine-based inhibitors of dipeptidyl peptidase IV and methods

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Page/Page column 35-36, (2008/06/13)

Compounds are provided having the formula (I) wherein R, X, Y, Z, A and n are as defined herein, which are inhibitors of dipeptidyl peptidase IV and thus are useful in treating diabetes and related diseases.

6-(((SUBSTITUTED)PYRIDIN-3-YL)ALKYL)-AND ALKENYL)-TETRAHYDRO-4-HYDROXYPYRAN-2-ONE INHIBITORS OF CHOLESTEROL BIOSYNTHESIS

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, (2008/06/13)

Certain trans-6-[[(substituted)pyridin-3-yl]-alkyl-and alkenyl] tetrahydro-4-hydroxypyran-2-ones and the corresponding ring-opened acids derived therefrom are potent inhibitors of the enzyme 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA reducta

Esters of phenalkyloxycarbonylamino acids

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, (2008/06/13)

Novel esters of phenylalkyloxy- or phenylalkylthioacylamino acids and pyridylalkyloxy- or pyridylalkylthioacylamino acids, synthesis thereof, intermediates therefor, and the use of said esters for the control of weeds.

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