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2H-Indol-2-one, 1,3-dihydro-3-(hydroxymethylene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63273-23-4

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63273-23-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63273-23-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,7 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63273-23:
(7*6)+(6*3)+(5*2)+(4*7)+(3*3)+(2*2)+(1*3)=114
114 % 10 = 4
So 63273-23-4 is a valid CAS Registry Number.

63273-23-4SDS

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 3-hydroxymethyleneindolin-2-one

1.2 Other means of identification

Product number -
Other names 3-(Hydroxymethylene)indolin-2-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:63273-23-4 SDS

63273-23-4Downstream Products

63273-23-4Relevant academic research and scientific papers

Total synthesis of spirotryprostatin B via diastereoselective prenylation

Trost, Barry M.,Stiles, Dylan T.

, p. 2763 - 2766 (2007)

Spirotryprostatin B was synthesized in eight steps, utilizing an efficient palladium-catalyzed prenylation reaction to construct the quaternary C3 stereocenter. The decarboxylation-alkylation of a series of substituted β-keto esters is described, demonstr

The Preparation of Synthetic Analogues of Strigol

Johnson, Alan W.,Gowda, Gopala,Hassanali, Ahmed,Knox, John,Monaco, Sam,et al.

, p. 1734 - 1743 (2007/10/02)

A range of analogues of the natural germination stimulant, strigol, for parasitic weeds of the genera Striga and Orobanche, has been prepared.Most of the products contain an α-formyl-γ-lactone (or α-formyl-γ-lactam) grouping attached through an enol-ether linkage to the 5-position of a but-2-enolide.Some have shown sufficiently high activities as to warrant large-scale field trials.

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