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77039-78-2

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77039-78-2 Usage

Description

2-Chromanecarbonylchloride, with the chemical formula C10H7ClO2, is a carbonyl chloride derivative of 2-chromene. It is a colorless liquid at room temperature and is highly reactive due to the presence of the carbonyl chloride functional group. 2-Chromanecarbonylchloride is a valuable tool for chemists in the development of new molecules and compounds, particularly in the synthesis of various heterocyclic compounds and organic intermediates.

Uses

Used in Pharmaceutical Industry:
2-Chromanecarbonylchloride is used as a reagent in organic synthesis for the production of pharmaceuticals. Its ability to undergo nucleophilic acyl substitution reactions makes it a valuable tool in the development of new molecules and compounds for medicinal applications.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Chromanecarbonylchloride is utilized as a reagent in the synthesis of various agrochemicals. Its reactivity and versatility in organic synthesis contribute to the development of new compounds for agricultural and pest control purposes.
Used in Fine Chemicals Production:
2-Chromanecarbonylchloride is also used in the production of other fine chemicals. Its role as a building block in the synthesis of heterocyclic compounds and organic intermediates highlights its importance in creating specialty chemicals for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 77039-78-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,3 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77039-78:
(7*7)+(6*7)+(5*0)+(4*3)+(3*9)+(2*7)+(1*8)=152
152 % 10 = 2
So 77039-78-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClO2/c11-10(12)9-6-5-7-3-1-2-4-8(7)13-9/h1-4,9H,5-6H2

77039-78-2SDS

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 Chromane-2-carbonyl chloride

1.2 Other means of identification

Product number -
Other names chroman-2-carbonyl chloride

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:77039-78-2 SDS

77039-78-2Relevant articles and documents

ANTAGONISTS OF THE TRPV1 RECEPTOR AND USES THEREOF

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Page/Page column 20, (2008/12/06)

The present application is directed to compounds that are TRPV1 antagonists and have formula (I) wherein variables Ar1, L1, R1, R2, R3, R4, R5, Y1, Y2, and Y3, are as defined in the description, which are useful for treating disorders caused by or exacerbated by vanilloid receptor activity.

SUBSTITUTED AMINOMETHYLTETRALINS AND THEIR HETEROCYCLIC ANALOGUES

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, (2008/06/13)

For binding 5-HT 1 receptors and thereby treating central nervous system disorders, novel substituted aminomethyltetralins and their heterocyclic analogues of the formula STR1 in which Z--denotes a group of the formula STR2 R 1, E and F can be hydrogen or other radicals, or salts thereof.

Pharmacomodulation d'adrenolytiques α en serie benzopyrannique

Mouysset, Genevieve,Payard, Marc,Grassy, Gerard,Tronche, Pierre,Dabire, Hubert,et al.

, p. 539 - 544 (2007/10/02)

Pharmacomodulation of α-adrenergic blocking agents by a series of benzopyrans.The N-methylpiperidine fragment was associated with four oxygenated heterocycles of the benzopyran ring system.Two different synthesis pathways were used in each case.Twenty intermediate derivatives and four aminomethylated derivatives whose structures were established by spectroscopic data are described.The pharmacological investigation demonstrates the interest of these compounds on the α-adrenergic receptors in light of their activities and selectivities. α1-adrenergic blocking agents / α2-adrenergic blocking agents / piperidinomethyl chromone, chromene and chromane

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