CasNo.20535-83-5,C6H7N5O 6-Methoxyguanine 20535-83-5,(20535-83-5) Suppliers

1 Metric Ton	Negotiable

Min.Order :1 Metric Ton
Purity: 99.5%
Payment Terms : L/C,T/T,

Keywords

6-Methoxyguanine 20535-83-5 C6H7N5O

Quick Details

Appearance:Powder
Application:20535-83-5
PackAge:Aluminium Foil Bag and Paper Drum
ProductionCapacity:100|Metric Ton|Day
Storage:1MT
Transportation:By Sea/Air/DHL

Superiority:

Our company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.Our main business covers the fields below:

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3.OLED intermediates (Fluorene,Carbazole,Boric acid...)

4.Customs Synthesis

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Details:

6-Methoxyguanine Basic information

Product Name:	6-Methoxyguanine
Synonyms:	O6-METHYLGUANINE;O-METHYLGUANINE;2-amino-6-methoxy-purin;6-methoxy-1h-purin-2-amin;6-methoxy-1h-purine-2-amine;o(sup6)-methylguanine;6-Methoxyguanine;6-methoxy-1h-purin-2-amine
CAS:	20535-83-5
MF:	C6H7N5O
MW:	165.16
EINECS:
Product Categories:	Amines;Purine;Chemical Amines;Purines;Bases & Related Reagents;Intermediates & Fine Chemicals;Nucleotides;Pharmaceuticals;Fused Ring Systems;Intermediate in the synthesis of Tropine and respective derivatives
Mol File:	20535-83-5.mol

6-Methoxyguanine Chemical Properties

Melting point	>300 °C(lit.)
CAS DataBase Reference	20535-83-5(CAS DataBase Reference)

Safety Information

Hazard Codes	Xi
Safety Statements	24/25
WGK Germany	3
RTECS	UO7473000
Hazard Note	Irritant

MSDS Information

Provider	Language
SigmaAldrich	English

6-Methoxyguanine Usage And Synthesis

Chemical Properties	Off-white solid
Uses	Antitumor agent
Definition	ChEBI: A methylguanine in which the methyl group is positioned on the oxygen at position 6. Formed in DNA by alkylation of the oxygen atom of guanine, most often by N-nitroso compounds and sometimes due to methylation by other compounds such as endogenous S-adenosylmethionine, it base-pairs to thymine rather than cytidine, causing a G:C to A:T transition in DNA.