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Phenol, 4-chloro-2-(1H-pyrrol-1-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59580-38-0

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59580-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59580-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,8 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 59580-38:
(7*5)+(6*9)+(5*5)+(4*8)+(3*0)+(2*3)+(1*8)=160
160 % 10 = 0
So 59580-38-0 is a valid CAS Registry Number.

59580-38-0SDS

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-chloro-2-pyrrol-1-ylphenol

1.2 Other means of identification

Product number -
Other names 4-chloro-2-pyrrol-1-yl-phenol

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:59580-38-0 SDS

59580-38-0Downstream Products

59580-38-0Relevant academic research and scientific papers

Pyrrolobenzoxazines, pyrrolobenzothiazines and process therefor

-

, (2008/06/13)

4H-Pyrrolo[2,1-c][1,4]benzoxazines and 4H-pyrrolo[2,1-c]-[1,4]benzothiazines characterized by having an alkylamine substituent at position 4 are disclosed. The compounds are characterized further by having an alkyl substituent on the same carbon atom bearing the alkylamine substituent. In addition the compounds may be optionally substituted at positions 1 and 6 to 9. Also disclosed are 4H-pyrrolo-[2,1-c][1,4]benzoxazines and 4H-pyrrolo[2,1-c][1,4]benzothiazines which are dialkylated at position 4 and have a methylamino substituent at position 1. The foregoing compounds possess antihypertensive and central nervous system depressant activity and methods for their preparation and use are described.

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