42236-50-0 Usage
Uses
Used in Fragrance Industry:
1,12-DIACETOXYDODECANE is used as a fragrance ingredient for its aromatic properties, contributing to the scent profiles of perfumes, soaps, and lotions. Its unique scent characteristics make it a valuable addition to the fragrance industry.
Used in Chemical Manufacturing:
1,12-DIACETOXYDODECANE serves as a solvent and a building block in the synthesis of other chemicals, playing a crucial role in the production of various chemical compounds.
Used in Consumer Products:
Beyond its aromatic applications, 1,12-DIACETOXYDODECANE is also utilized in the formulation of consumer products, enhancing their performance and functionality.
Safety Precautions:
Due to its potential to cause irritation to the skin, eyes, and respiratory system, as well as the possible harmful effects of prolonged exposure, 1,12-DIACETOXYDODECANE should be handled with care. Adequate safety measures and precautions are essential when working with this chemical to ensure the health and safety of individuals involved in its production, use, and handling.
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 academic research and scientific papers
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
SYNTHESIS OF (Z)-TETRADEC-11-EN-1-OL AND (Z)-HEXADEC-11-EN-1-OL FROM DODECANE-1,12-DIOL
Zakharkin, L. I.,Guseva, V. V.
, p. 733 - 736 (2007/10/02)
A method have been developed for obtaining (Z)-tetradec-11-en-1-ol and (Z)-hexadec-11-en-1-ol via dodec-11-yn-1-ol.
