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CAS

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866767-08-0

4-Amino-7-bromoisoindolin-1-one is a pale yellow solid organic compound with the molecular formula C8H6BrNO2. It belongs to the class of isoindolinones, which are cyclic compounds containing an isoindoline moiety. This chemical is insoluble in water and most organic solvents. The presence of the amino and bromo functional groups in this compound makes it chemically reactive and versatile for use in chemical reactions and organic synthesis.

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  • 866767-08-0 Structure

  • Basic information

    1. Product Name: 4-AMino-7-broMoisoindolin-1-one
    2. Synonyms: 4-AMino-7-broMoisoindolin-1-one;4-Amino-7-bromo-2,3-dihydro-1H-isoindol-1-one;1H-Isoindol-1-one, 4-aMino-7-broMo-2,3-dihydro-
    3. CAS NO:866767-08-0
    4. Molecular Formula: C8H7BrN2O
    5. Molecular Weight: 227.05798
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 866767-08-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.753
    6. Refractive Index: N/A
    7. Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-AMino-7-broMoisoindolin-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-AMino-7-broMoisoindolin-1-one(866767-08-0)
    11. EPA Substance Registry System: 4-AMino-7-broMoisoindolin-1-one(866767-08-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 866767-08-0(Hazardous Substances Data)

866767-08-0 Usage

Uses

Used in Pharmaceutical Industry:
4-Amino-7-bromoisoindolin-1-one is used as an intermediate in the synthesis of pharmaceuticals for its chemical reactivity and versatility. It plays a crucial role in the development of new drugs and medications.
Used in Agrochemical Industry:
4-Amino-7-bromoisoindolin-1-one is used as an intermediate in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals.
Used in Organic Synthesis:
4-Amino-7-bromoisoindolin-1-one is used as a building block for various organic compounds due to its chemical reactivity and the presence of functional groups. It aids in the creation of new organic molecules for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 866767-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,7,6 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 866767-08:
(8*8)+(7*6)+(6*6)+(5*7)+(4*6)+(3*7)+(2*0)+(1*8)=230
230 % 10 = 0
So 866767-08-0 is a valid CAS Registry Number.

866767-08-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Amino-7-bromo-1-isoindolinone

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:866767-08-0 SDS

866767-08-0Downstream Products

866767-08-0Relevant articles and documents

HPK1 ANTAGONISTS AND USES THEREOF

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Paragraph 1338; 1342, (2021/03/19)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of HPK1, and the treatment of HPK1-mediated disorders.

BICYCLIC AROMATIC RING DERIVATIVES OF FORMULA (I) AS ATF4 INHIBITORS

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, (2019/10/29)

The invention is directed to substituted bicyclic aromatic derivatives. Specifically, the invention is directed to compounds according to Formula (I) wherein A, C, D, L2, L3, R1, R2, R3, R4

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