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164178-39-6

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164178-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 164178-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,1,7 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 164178-39:
(8*1)+(7*6)+(6*4)+(5*1)+(4*7)+(3*8)+(2*3)+(1*9)=146
146 % 10 = 6
So 164178-39-6 is a valid CAS Registry Number.

164178-39-6SDS

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 (2S,3S,4S,5R,6S)-6-[[[(Z)-[2-(dimethylamino)-1-methylsulfanyl-2-oxoethylidene]amino]oxycarbonyl-methylamino]methoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

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:164178-39-6 SDS

164178-39-6Downstream Products

164178-39-6Relevant articles and documents

Phloem Mobility of Xenobiotics VI. A Phloem-Mobile Pro-nematicide Based on Oxamyl Exhibiting Root-Specific Activation in Transgenic Tobacco

Hsu, Francis C.,Sun, Kingmo,Kleier, Daniel A.,Fielding, Max J.

, p. 9 - 20 (1995)

Phloem mobility is a desirable attribute for pesticides in many applications, and the physicochemical properties necessary for phloem mobility are now well understood. However, attempts to derivatize pesticides to make them phloem mobile are often frustrated by a concomitant loss of activity. This study describes a phloem-mobile pro-nematicide, a hydroxymethyloxamyl glucuronide (JR522) coupled with an in-situ activation mechanism in transgenic tobacco expressing Escherichia coli β-glucuronidase in its root tips. When applied foliary to the transgenic tobacco, JR522 and its methyl ester (JM775) showed greater nematicidal activity than oxamyl against root-knot nematodes. This example of combining pro-pesticide chemistry with crop genetic engineering for site-specific activation provides a model system for demonstrating how to circumvent the often mutual exclusivity of phloem mobility and pesticidal activity. Additional advantages of this scheme include the potential mammalian safety of the pro-pesticide, as exhibited by JR522 in this study, and a high degree of site-specific release of xenobiotics in plants.

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