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92964-91-5

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92964-91-5 Usage

Chemical class

Xanthene derivative

Field of use

Organic chemistry

Known for

Fluorescent properties

Utilized as

Fluorescent dye

Applications

Bioimaging, fluorescence microscopy

Structure

Xanthene core with a prop-2-en-1-yloxy group attached

Chemical and physical properties

Unique due to the prop-2-en-1-yloxy group

Potential uses

Development of new materials and technologies, research and development in life sciences

Check Digit Verification of cas no

The CAS Registry Mumber 92964-91-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,6 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92964-91:
(7*9)+(6*2)+(5*9)+(4*6)+(3*4)+(2*9)+(1*1)=175
175 % 10 = 5
So 92964-91-5 is a valid CAS Registry Number.

92964-91-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-prop-2-enoxyxanthen-9-one

1.2 Other means of identification

Product number -
Other names 1-allyloxy-xanthen-9-one

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:92964-91-5 SDS

92964-91-5Downstream Products

92964-91-5Relevant articles and documents

An Efficient Two-Step Protocol for the Isoprenylation of Xanthone at the C2 Position Starting from 1-Fluoroxanthone Derivative

Fujimoto, Yuuki,Furukawa, Chisato,Takahashi, Kanae,Mochizuki, Miho,Yanai, Hikaru,Matsumoto, Takashi

, p. 1423 - 1429 (2020/11/23)

The S NAr reaction of 1-fluoroxanthone derivatives with alkoxide of 1,1-dimethylallyl alcohol cleanly afforded the corresponding ethers, which have thus far been unavailable. The obtained ethers underwent the Claisen rearrangement at room tempe

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