6225-06-5 Usage
General Description
N,N-Dimethylvaleramide is a chemical compound that belongs to the family of valeramide derivatives. It is a colorless to light yellow liquid with a characteristic odor. N,N-DIMETHYLVALERAMIDE is commonly used as a solvent and a precursor in the production of various industrial chemicals, including pharmaceuticals and agrochemicals. It is also used as a reagent in organic synthesis and as an intermediate in the production of fragrances and flavors. N,N-Dimethylvaleramide is known for its low toxicity and has a relatively low environmental impact, making it a versatile and valuable compound in various industrial applications. However, it should be handled with care, as prolonged or repeated exposure may cause irritation to the skin, eyes, and respiratory system.
Check Digit Verification of cas no
The CAS Registry Mumber 6225-06-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,2 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6225-06:
(6*6)+(5*2)+(4*2)+(3*5)+(2*0)+(1*6)=75
75 % 10 = 5
So 6225-06-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO/c1-4-5-6-7(9)8(2)3/h4-6H2,1-3H3
6225-06-5Relevant articles and documents
Carboxamidation of Organolithium and Organomagnesium Reagents by a Two-Step One-Flask Reaction. Promotion by Magnesium Alkoxides
Screttas, Constantinos G.,Steele, Barry R.
, p. 5151 - 5153 (1988)
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Direct catalytic formation of primary and tertiary amides from non-activated carboxylic acids, employing carbamates as amine source
Tinnis, Fredrik,Lundberg, Helena,Adolfsson, Hans
supporting information, p. 2531 - 2536 (2012/11/06)
The operationally simple titanium(IV)- or zirconium(IV)-catalyzed direct amidation of non-activated carboxylic acids with ammonium carbamates generates primary, and tertiary N,N-dimethyl-substituted amides in good to excellent yields. Copyright
Vinyl-λ3-iodanes act as efficient sulfur atom acceptors: Vinylic SN2-based strategy for conversion of tertiary thioamides to amides
Ochiai, Masahito,Yamamoto, Shinji
, p. 2802 - 2803 (2007/10/03)
Exposure of tertiary thioamides to (E)-1-hexenyl(phenyl)-λ3-iodane results in vinylic SN2 reaction to give the inverted (Z)-S-vinylthioimidonium salts, which under alkaline hydrolysis (Na2CO3 or K2CO
