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2851-80-1

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2851-80-1 Usage

General Description

2,7-dimethyl-9H-fluorene is a polycyclic aromatic hydrocarbon compound with the chemical formula C15H12. It is a white to off-white crystalline solid that is insoluble in water but soluble in organic solvents. 2,7-dimethyl-9H-fluorene is commonly used as a building block in the synthesis of various organic compounds, including pharmaceuticals, dyes, and polymers. It is considered to be a hazardous chemical, as it is a suspected carcinogen and can cause irritation and damage to the respiratory system if inhaled. Additionally, 2,7-dimethyl-9H-fluorene is flammable and may release toxic fumes when heated to decomposition. Therefore, appropriate safety precautions should be taken when handling and storing this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 2851-80-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,5 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2851-80:
(6*2)+(5*8)+(4*5)+(3*1)+(2*8)+(1*0)=91
91 % 10 = 1
So 2851-80-1 is a valid CAS Registry Number.

2851-80-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-dimethyl-9H-fluorene

1.2 Other means of identification

Product number -
Other names 2,7-Dimethylfluorene

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:2851-80-1 SDS

2851-80-1Relevant articles and documents

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Alt, Helmut G.,Zenk, Roland

, p. 39 - 54 (2007/10/03)

Seventeen new catalyst precursors for the syndiospecific polymerization of propylene are presented. The new metallocene complexes are substituted in the positions 2 and 7 of the fluorenylidene fragment by MeO-, halogen-, alkyl-and aryl groups. The focus i

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