42236-50-0 Usage
General Description
1,12-DIACETOXYDODECANE is a chemical compound with the molecular formula C16H30O4. It is a derivative of dodecane, with two acetoxy groups attached to the 1 and 12 positions of the carbon chain. This chemical is commonly used as a fragrance ingredient and can be found in various consumer products such as perfumes, soaps, and lotions. It is also used as a solvent and in the manufacturing of other chemicals. However, 1,12-DIACETOXYDODECANE should be handled with care as it can cause irritation to the skin, eyes, and respiratory system, and prolonged exposure may have harmful effects on health. Therefore, proper safety measures and precautions should be taken when working with this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 42236-50-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,3 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 42236-50:
(7*4)+(6*2)+(5*2)+(4*3)+(3*6)+(2*5)+(1*0)=90
90 % 10 = 0
So 42236-50-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H30O4/c1-15(17)19-13-11-9-7-5-3-4-6-8-10-12-14-20-16(2)18/h3-14H2,1-2H3
42236-50-0Relevant articles and documents
The preparation of three new partially deuterated hexadecanethiols for applications in surface chemistry
Sheepwash, Erin E.,Rowntree, Paul A.,Schwan, Adrian L.
experimental part, p. 391 - 398 (2009/04/07)
The synthesis of three partially deuterated hexadecanethiols has been achieved. Thiols CH3(CH2)7(CD2) 8SH, CD3(CD2)7(CH2) 8SH and CD3(CH2)15SH were targeted, as these compounds, after formation of self-assembled monolayers on Au(1 1 1) or Au nanoparticles, can provide mechanistic information pertaining to reactive atom migrations within the assembly. The syntheses of each of these compounds called upon Grignard coupling chemistry, which was activated by Li 2CuCl4. Applicable deuterium containing fragments were either commercially obtained or constructed from by way of an inexpensive and efficient ring opening, protection and dimerization of THF-d8. Sulfur incorporation was by thiolacetate substitution or addition reactions. The protocols presented possess general applicability in a number of syntheses requiring block-deuterated fattyalkyl sections. Copyright
