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2,3:5,6-bis-O-(1-Methylethylidene)-L-gulose oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

420846-29-3

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420846-29-3 Usage

Source

It is derived from maize and other grasses.

Function

It acts as a deterrent to herbivores and insects.

Anti-herbivore and anti-pathogen activities

Studies have shown that DIMBOA oxime exhibits inhibitory effects on the growth of certain pathogens and pests.

Agricultural and pharmaceutical applications

It has potential applications in the development of natural pesticides and herbicides.

Potential value

It is a potentially valuable compound for agricultural and pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 420846-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,0,8,4 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 420846-29:
(8*4)+(7*2)+(6*0)+(5*8)+(4*4)+(3*6)+(2*2)+(1*9)=133
133 % 10 = 3
So 420846-29-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H21NO6/c1-11(2)16-6-8(18-11)9(14)10-7(5-13-15)17-12(3,4)19-10/h5,7-10,14-15H,6H2,1-4H3/b13-5+/t7-,8+,9-,10-/m1/s1

420846-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3:5,6-O-diisopropylidene-L-gulose oxime

1.2 Other means of identification

Product number -
Other names -

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:420846-29-3 SDS

420846-29-3Relevant academic research and scientific papers

Stereoselective synthesis of tubuvaline methyl ester and tubuphenylalanine, components of tubulysins, tubulin polymerization inhibitors

Shibue, Taku,Hirai, Toshihiro,Okamoto, Iwao,Morita, Nobuyoshi,Masu, Hyuma,Azumaya, Isao,Tamura, Osamu

scheme or table, p. 3845 - 3848 (2009/10/11)

Synthetic studies of two components of tubulysins, tubulin polymerization inhibitors are described. The highly stereoselective synthesis of tubuvaline methyl ester (2) was accomplished by 1,3-dipolar cycloaddition of nitrone d-6 and acrylic acid derivativ

Potential Glycosidase Inhibitors: Synthesis of 1,4-Dideoxy-1,4-imino Derivatives of D-Glucitol, D- and L-Xylitol, D- and L-Allitol, D- and L-Talitol, and D-Gulitol

Buchanan, J. Grant,Lumbard, Keith W.,Sturgeon, Robert J.,Thompson, Deryk K.

, p. 699 - 706 (2007/10/02)

Conversion of 2,3,5,6-tetra-O-benzyl-D-galactofuranose (19) into its oxime and subsequent treatment with methanesulphonyl chloride gave 2,3,5,6-tetra-O-benzyl-4-O-methylsulphonyl-D-galactonitrile (21).Reductive cyclization by sodium borohydride/cobalt(II)

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