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2504-18-9

2504-18-9

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  • 2H-3,9a-Methano-1-benzoxepin-9-methanol,3,4,5,5a,6,7-hexahydro-2,2,5a-trimethyl-, (3R,5aS,9aR)-

    Cas No: 2504-18-9

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2504-18-9 Usage

Uses

N-Nitroso-methyl-tertbutyl-amine is used in the rubber industry.

Check Digit Verification of cas no

The CAS Registry Mumber 2504-18-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,0 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2504-18:
(6*2)+(5*5)+(4*0)+(3*4)+(2*1)+(1*8)=59
59 % 10 = 9
So 2504-18-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H12N2O/c1-5(2,3)7(4)6-8/h1-4H3

2504-18-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-tert-butyl-N-methylnitrous amide

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:2504-18-9 SDS

2504-18-9Upstream product

2504-18-9Relevant articles and documents

Metal-Free Cycloetherification by in Situ Generated P-Stereogenic α-Diazanium Intermediates: A Convergent Synthesis of Enantiomerically Pure Dihydrobenzooxaphospholes

Li, Shi-Guang,Han, Zhengxu S.,Viereck, Peter,Lee, Heewon,Kurouski, Dmitry,Senanayake, Chris H.,Tsantrizos, Youla S.

, p. 894 - 897 (2017)

A metal-free tandem reaction, initiated by the generation of a diazonium cation and followed by cycloetherification, was developed. Acid-promoted de-tert-butylation of N-nitroso N-tert-butylamine was used to generate a diazonium cation in situ, demonstrating a new application of nitroso chemistry. This reaction was employed in the synthesis of substituted benzofuran-3(2H)-ones and dihydrobenzo[d][1,3]oxaphosphole 3-oxides.

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