37110-18-2 Usage
Uses
Used in Industrial Applications:
1,3-dihydroxyacetone oxime is used as a chelating agent in various industrial processes for its ability to bind with metal ions, which helps in preventing unwanted chemical reactions and improving the efficiency of certain processes.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 1,3-dihydroxyacetone oxime is used as a key intermediate in the synthesis of various drugs, contributing to the development of new medicinal compounds.
Used in Organic Synthesis:
1,3-dihydroxyacetone oxime is utilized as a reagent in the synthesis of organic compounds, especially in the formation of nitrogen-containing heterocyclic compounds, which are important in various chemical and pharmaceutical applications.
Used in Cosmetics as a Tanning Agent:
In the cosmetics industry, 1,3-dihydroxyacetone oxime is used as a tanning agent. It reacts with amino acids in the skin to produce a temporary bronze color, providing a safe and effective alternative to sun exposure for achieving a tanned appearance.
Check Digit Verification of cas no
The CAS Registry Mumber 37110-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,1,1 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 37110-18:
(7*3)+(6*7)+(5*1)+(4*1)+(3*0)+(2*1)+(1*8)=82
82 % 10 = 2
So 37110-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H7NO3/c5-1-3(2-6)4-7/h5-7H,1-2H2
37110-18-2Relevant articles and documents
Kinetics and Mechanism of the Alkaline Release of Phenyl(mercapto)tetrazoles from α-Oximes
Boggs, Roger A.,Hasan, Fariza B.,Mahoney, J. Barry,Mehta, Avi C.,Palumbo, Catherine M. K.,et al.
, p. 1271 - 1277 (2007/10/02)
Compounds such as α-phenyl(mercapto)tetrazole (PMT) oxime (9) undergo rapid elimination of the PMT anion in base via a nitrosoene intermediate.Solution kinetics and HPLC analysis of reaction products are consistent with the mechanism shown in Scheme 2.For open chain oximes such as 4, substitution α to the oxime increases the rate of release of PMT and is attributed to the relief of strain when a crowded reactant is converted to a less-crowded product.For cyclic oximes, the six-membered ring compounds are more reactive than the corresponding five-membered compounds.A linear isokinetic relationship between the entropy and enthalpy of activation was found with β = 346 +/- 51 K.Entropies of activation were found to range from -7 to +24 c.u. (1 c.u. = 4.184 J mol-1 K-1) and support the proposed mechanism.
