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Bromomethane-d1 (gas), also known as CH3Br-d1, is a deuterated form of bromomethane, a halogenated hydrocarbon. It is a colorless, flammable, and toxic gas with a molecular weight of 97.94 g/mol. Bromomethane-d1 is primarily used as a chemical intermediate in the synthesis of various organic compounds, as well as a tracer in chemical reactions and a reagent in isotopic labeling studies. Due to its hazardous nature, it is essential to handle and store bromomethane-d1 with proper safety measures, including the use of appropriate personal protective equipment and containment systems.

1861-05-8

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1861-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1861-05-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,6 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1861-05:
(6*1)+(5*8)+(4*6)+(3*1)+(2*0)+(1*5)=78
78 % 10 = 8
So 1861-05-8 is a valid CAS Registry Number.

1861-05-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name bromo(deuterio)methane

1.2 Other means of identification

Product number -
Other names Mondeuterio-monobrom-methan

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:1861-05-8 SDS

1861-05-8Downstream Products

1861-05-8Relevant academic research and scientific papers

Controlled formation of tetramethylammonium mono- and diylide

Cristau, Henri-Jean,Plenat, Francoise,Bayssade, Sylvie

, p. 29 - 33 (2007/10/03)

The reaction of tetramethylammonium bromide with n -butyllithium can selectively yield either trimethylammonium methylide or lithium dimethylammonium dimethylide, depending on the reaction conditions, as shown by 13C-NMR analysis of the deuterium-labelled species resulting from acidic trapping with DCl. So a simple synthesis of mono- or twice-functionalised methylammonium salts is allowed from a very usual starting material.

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