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2,4(1H,3H)-Pyrimidinedione, 6-[(3,5-dimethylphenyl)methylamino]-3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88200-84-4

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88200-84-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88200-84-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,0 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88200-84:
(7*8)+(6*8)+(5*2)+(4*0)+(3*0)+(2*8)+(1*4)=134
134 % 10 = 4
So 88200-84-4 is a valid CAS Registry Number.

88200-84-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3',5',N'-tetramethyl-6-(phenylamino)-2,4-(1H,3H)-pyrimidinedione

1.2 Other means of identification

Product number -
Other names 6-(N-methyl-3,5-xylidino)-3-methyluracil

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:88200-84-4 SDS

88200-84-4Downstream Products

88200-84-4Relevant academic research and scientific papers

Fluid Solution and Solid-State Electron Nuclear Double Resonance Studies of Flavin Model Compounds and Flavoenzymes

Kurreck, H.,Bock, M.,Bretz, N.,Elsner, M.,Kraus, H.,et al.

, p. 737 - 746 (2007/10/02)

Partially deuterated and various substituted flavin and thiaflavin model compounds have been synthesized.For the first time, high-resolution H, D, and 14N ENDOR and TRIPLE resonance experiments in fluid solution have been performed on the paramagnetic derivatives of these compounds.Additionally, valuable information has been obtained about hyperfine anisotropies and molecular structures from ENDOR in rigid matrices.Solid matrix ENDOR studies of native flavoenzymes, namely, "Old Yellow Enzyme" (NADPH dehydrogenase), two flavodoxins, and a methanol oxidase are reported.The ENDOR matrix signals of the various flavoproteins are different in intensity, suggesting that the microenvironments are remarkably different.Applicabilities and limitations of the ENDOR technique in the studies of flavins and flavoenzymes are discussed.

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