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Chloromethane-d2, also known as CDM or CH3DCl, is a deuterated form of chloromethane, a simple organic compound with the formula CH3Cl. In chloromethane-d2, the hydrogen atoms are replaced with deuterium atoms, resulting in a molecular formula of CD3Cl. chloromethane-d2 is primarily used as a reagent in organic synthesis, particularly in the preparation of isotopically labeled compounds for research purposes. It is also utilized in the production of deuterated solvents and as a tracer in chemical reactions to study reaction mechanisms and kinetics. Due to its deuterated nature, chloromethane-d2 is less reactive than its non-deuterated counterpart, which can be advantageous in certain applications where reduced reactivity is desired.

4960-87-6

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4960-87-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4960-87-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,6 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4960-87:
(6*4)+(5*9)+(4*6)+(3*0)+(2*8)+(1*7)=116
116 % 10 = 6
So 4960-87-6 is a valid CAS Registry Number.

4960-87-6Downstream Products

4960-87-6Relevant academic research and scientific papers

Kinetics of reactions of CN with chlorinated methanes

Samant, Vaishali,Hershberger, John F.

, p. 64 - 67 (2008)

The kinetics of reactions of CN with the chlorinated methanes CH3Cl, CH2Cl2, CHCl3 and CCl4 were investigated over the temperature range 298-573 K, using laser induced fluorescence (LIF) spectroscopy. At 298 K, rate constants of 9.0 ± 0.3 × 10-13, 8.8 ± 0.4 × 10-13, 9.0 ± 0.5 × 10-13 and 4.3 ± 0.6 × 10-13 cm3 molecule-1 s-1 were measured, respectively. A small positive temperature dependence was observed, as well as kinetic isotope effects of kH/kD ~ 2.14-2.25. These data along with product detection experiments strongly suggest that hydrogen abstraction dominates these reactions.

Onium Ylide Chemistry. 4. Alkylhalonium Methylides

Olah, George A.,Doggweiler, Hans,Felberg, Jeff D.

, p. 4975 - 4978 (2007/10/02)

Alkylhalonium methylides were generated by two independent routes, proving their formation through derived product analysis.The reaction of singlet methylene, produced by photolysis of diazomethane, with methyl and ethyl halides gives in competition with C-H insertion evidence of methylenation of halogen atom, i.e., alkylhalonium methylide formation.The unstable halonium methylides are immediatly protonated or alkylated in the reaction medium to give dialkylhalonium ions which then undergo cleavage to the corresponding alkyl halides.Methyliodonium methylide was also generated via the deprotonation of dimethyliodonium hexafluoroantimonate with sodium hydride in competition with the expected methylation of fluoride and hydride, giving the major products.Subsequent methylation of the methyliodonium methylide by excess dimethyliodonium ion gives methylethyliodonium ion followed by cleavage leading to the formation of ethyl halides and via hydride reduction to ethane, respectively.Attempted formation of alkylhalonium methylides via fluoride cleavage of methylhalonium hexafluoroantimonates was unsuccessful due to ready disproportionation of the halonium ions.

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