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16206-18-1

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16206-18-1 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 33, p. 2086, 1968 DOI: 10.1021/jo01269a082

Check Digit Verification of cas no

The CAS Registry Mumber 16206-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,0 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16206-18:
(7*1)+(6*6)+(5*2)+(4*0)+(3*6)+(2*1)+(1*8)=81
81 % 10 = 1
So 16206-18-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H3N5O2/c5-3-2-4(7-1-6-3)8-11-9(2)10/h1H,(H2,5,6,7,8)

16206-18-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-oxido-[1,2,5]oxadiazolo[3,4-d]pyrimidin-1-ium-7-amine

1.2 Other means of identification

Product number -
Other names [1,2,5]oxadiazolo[3,4-d]pyrimidin-7-amine 1-oxide

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:16206-18-1 SDS

16206-18-1Downstream Products

16206-18-1Relevant articles and documents

Pyrazine-1,4-dioxides fused to heterocyles. 3rd comm. Synthesis and antibacterial activity of substituted pteridine-5,8-dioxides

Binder,Noe,Prager,Turnowsky

, p. 803 - 805 (2007/10/02)

The synthesis of substituted pteridine-5,8-dioxides via reaction of furoxanes with enolizing carbonyl compounds is described. Compounds 5 are obtained either through reaction of chloro pyrimidines 1 with sodium azide, or through diazotization of hydrazino pyrimidine 2 and subsequent thermal decomposition of 3 or through nucleophilic displacement of methoxy against amino groups in 5. The antibacterial activity of the compounds 6a and 6c is directed against some gramnegative organisms, i.e. E. coli, Klebsiella spp. and Proteus spp., with MIC values and ED50 values which do not exceed those of the corresponding pyrido[2,3-b]pyrazine-1,4-dioxides.

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