332134-60-8 Usage
Uses
Used in Pharmaceutical Industry:
Morpholine, 4-(6-bromo-2-pyridinyl)is used as a key intermediate in the synthesis of pharmaceuticals for its potential to contribute to the development of bioactive molecules. Its unique structure allows for the creation of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, Morpholine, 4-(6-bromo-2-pyridinyl)serves as a building block for the synthesis of agrochemicals, potentially enhancing the effectiveness of pesticides, herbicides, and other agricultural products by incorporating its unique chemical properties.
Used as a Corrosion Inhibitor in Oil and Gas Industry:
Morpholine, 4-(6-bromo-2-pyridinyl)is utilized as a corrosion inhibitor to protect metal equipment in the harsh environments of the oil and gas industry. Its ability to prevent corrosion extends the lifespan of equipment and reduces maintenance costs, making it a valuable asset in this sector.
Check Digit Verification of cas no
The CAS Registry Mumber 332134-60-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,1,3 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 332134-60:
(8*3)+(7*3)+(6*2)+(5*1)+(4*3)+(3*4)+(2*6)+(1*0)=98
98 % 10 = 8
So 332134-60-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H11BrN2O/c10-8-2-1-3-9(11-8)12-4-6-13-7-5-12/h1-3H,4-7H2
332134-60-8Relevant academic research and scientific papers
Quinuclidine compounds and drugs containing the same as the active ingredient
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, (2008/06/13)
The present invention provides an excellent squalene synthesizing enzyme inhibitor. Specifically, it provides a compound (I) represented by the following formula, a salt thereof or a hydrate of them. In which R1 represents (1) hydrogen atom or (2) hydroxyl group; HAr represents an aromatic heterocycle which may be substituted with 1 to 3 groups; Ar represents an optionally substituted aromatic ring; W represents a chain represented by (1) —CH2—CH2— which may be substituted, (2) —CH=CH— which may be substituted, (3) —C≡C—, (4) —NH—CO—, (5) —CO—NH—, (6) —NH—CH2—, (7) —CH2—NH—, (8) —CH2—CO—, (9) —CO—CH2—, (10) —NH—S(O)l—, (11) —S(O)l—NH—, (12) —CH2—S(O)— or (13) —S(O)l—CH2— (l denotes 0, 1 or 2); and X represents a chain represented by (1) a single bond, (2) an optionally substituted C1-6 alkylene chain, (3) an optionally substituted C2-6 alkenylene chain, (4) an optionally substituted C2-6 alkynylene chain, (5) a formula —Q— (wherein Q represents oxygen atom, sulfur atom, CO or N(R2) (wherein R2 represents a C1-6 alkyl group or a C1-6 alkoxy group)), (6) —NH—CO—, (7) —CO—NH—, (8) —NH—CH2—, (9) —CH2—NH—, (10) —CH2—CO—, (11) —CO—CH2—, (12) —NH—S(O)m—, (13) —S(O)m—NH—, (14) —CH2—S(O)m—, (15) —S(O)m—CH2— (wherein m denotes 0, 1 or 2) or (16) —(CH2)n—O— (wherein n denotes an integer from 1 to 6).
