861299-14-1 Usage
General Description
4-Chloro-2-methoxyaniline, HCl is a chemical compound that consists of a substituted aniline molecule with a chlorine atom and a methoxy group attached to the benzene ring, as well as a hydrochloric acid molecule. 4-Chloro-2-methoxyaniline, HCl is commonly used in the synthesis of pharmaceuticals, agrochemicals, and dyes. It is also used as an intermediate in the production of other organic compounds. The hydrochloric acid component of the compound provides stability and solubility in water, making it easier to handle and use in various chemical processes. Additionally, the 4-Chloro-2-methoxyaniline component contributes to the compound's reactivity and utility in organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 861299-14-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,1,2,9 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 861299-14:
(8*8)+(7*6)+(6*1)+(5*2)+(4*9)+(3*9)+(2*1)+(1*4)=191
191 % 10 = 1
So 861299-14-1 is a valid CAS Registry Number.
861299-14-1Relevant articles and documents
Synthesis and characterization of bis(4-amino-2-bromo-6-methoxy)azobenzene derivatives
Martínez-López, David,Babalhavaeji, Amirhossein,Sampedro, Diego,Andrew Woolley
, p. 3000 - 3008 (2019)
Aminoazobenzene derivatives with four ortho substituents with respect to the N-N double bond are a relatively unexplored class of azo compounds that show promise for use as photoswitches in biology. Tetra-ortho-methoxy-substituted aminoazobenzene compounds in particular can form azonium ions under physiological conditions and exhibit red-light photoswitching. Here, we report the synthesis and characterization of two bis(4-amino-2-bromo-6-methoxy)azobenzene derivatives. These compounds form red-light-absorbing azonium ions, but only under very acidic conditions (pH a makes the azonium form unsuitable, the neutral versions of these compounds undergo trans-to-cis photoisomerization with blue-green light and exhibit slow (τ1/2 ≈ 10 min) thermal reversion and so may find applications under physiological conditions.
