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890408-44-3

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890408-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 890408-44-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,0,4,0 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 890408-44:
(8*8)+(7*9)+(6*0)+(5*4)+(4*0)+(3*8)+(2*4)+(1*4)=183
183 % 10 = 3
So 890408-44-3 is a valid CAS Registry Number.

890408-44-3SDS

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 2-Butanone, 4-(4-methoxy-1H-indol-3-yl)-

1.2 Other means of identification

Product number -
Other names 2-BUTANONE,4-(4-METHOXY-1H-INDOL-3-YL)-

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:890408-44-3 SDS

890408-44-3Downstream Products

890408-44-3Relevant articles and documents

Boron-Catalyzed Dehydrative Friedel-Crafts Alkylation of Arenes Using β-Hydroxyl Ketone as MVK Precursor

San, Htet Htet,Huang, Jie,Lei Aye, Seinn,Tang, Xiang-Ying

supporting information, p. 2386 - 2391 (2021/01/04)

Boron-catalyzed environmentally benign dehydrative Friedel-Crafts alkylation of indole/pyrrole and aniline derivatives with β-hydroxyl ketones has been developed for the first time. This method provides an efficient and green replacement of toxic and unst

Silica-supported sodium sulfonate with ionic liquid: A neutral catalyst system for Michael reactions of indoles in water

Gu, Yanlong,Ogawa, Chikako,Kobayashi, Shu

, p. 175 - 178 (2007/10/03)

(Chemical Equation Presented) A neutral catalytic system for Michael reactions of indoles has been developed by combining silica-supported benzenesulfonic acid sodium salt with hydrophobic ionic liquid in water. An efficient hydrophobic environment could

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