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Iodoform-D, also known as CHD2I, is a deuterated form of iodoform, a chemical compound with the formula CHD2I or CH2I2. It is a yellow crystalline solid that is used as a reagent in organic chemistry, particularly in the detection of aldehydes and ketones. Iodoform-D is synthesized by reacting acetone with iodine and a base, such as sodium hydroxide, in the presence of deuterium oxide (D2O) instead of water, which results in the incorporation of deuterium atoms into the molecule. This deuterated version is useful for studying reaction mechanisms and for applications in nuclear magnetic resonance (NMR) spectroscopy, where it can provide valuable information about the structure and dynamics of molecules.

2787-27-1

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2787-27-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2787-27-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,8 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2787-27:
(6*2)+(5*7)+(4*8)+(3*7)+(2*2)+(1*7)=111
111 % 10 = 1
So 2787-27-1 is a valid CAS Registry Number.
InChI:InChI=1/CHI3/c2-1(3)4/h1H/i1D

2787-27-1SDS

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 deuterio(triiodo)methane

1.2 Other means of identification

Product number -
Other names Triiodomethane-d

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:2787-27-1 SDS

2787-27-1Downstream Products

2787-27-1Relevant academic research and scientific papers

Photochemical reactions of 1-naphthylamines and haloforms: Formation of bis(4-amino-1-naphthyl)methylium salts with remarkably long-wave electronic absorption

Maeda, Koko,Horikoshi, Yumiko,Hayashi, Mariko,Mori, Yukie,Nagano, Hajime

, p. 789 - 792 (2007/10/03)

The photochemical colour change from colourless to green of N-substituted 1-naphthylamines 1a-c in CH2Cl2 containing a haloform was found to be irreversible, although optically active 3-(1-naphthylamino)camphor 1a had been reported t

High-Field NMR Determination of Magnetic Susceptibility Tensors and Angular Correlation Factors of Halomethanes

Bothner-By, A. A.,Dadok, J.,Mishra, P. K.,Zijl, P. C. M. Van

, p. 4180 - 4184 (2007/10/02)

Quadropolar splittings in the high resolution deuteron spectra of deuterated haloforms (CX3(2)H, X=Cl, Br, I) and methylene halides (CX2H(2)H) have been measured at 14.35 T (93.5 MHz) and used to determine the anisotropy or asymmetry of their molecular magnetic susceptibility tensors.By combination with the known isotropic susceptibilities, the principal susceptibility tensors have been deduced and decomposed into bond susceptibility tensors.Neither the average susceptibilities nor the principal susceptibility tensor elements of the complete halomethane series follow Pascal's additivity rules.The phenomenon is tentatively attributed to a variable paramagnetic contribution perpendicular to the X-bond.Angular correlation Kirkwood g2 factors have been determined for CHCl3 and CHBr3 and are compared with available literature data.

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