20:
122:
163:
182:
187:
156:
23:
90:
192:
111:
197:
149:
66:
19:
107:
National
Institute of Standards and Technology (NIST) reference data for anisoyl chloride
133:
176:
106:
58:
50:
121:
129:
70:
62:
54:
94:
74:
137:
97:group on the ring as compared to the acyl halide.
157:
8:
164:
150:
18:
89:forms. Their structures differ in the
57:acyl chloride, and may be formed from
7:
118:
116:
14:
34:(3-methoxybenzoyl chloride), and
120:
1:
30:(2-methoxybenzoyl chloride),
136:. You can help Knowledge by
38:(4-methoxybenzoyl chloride)
16:Group of chemical compounds
214:
115:
91:arene substitution pattern
183:Aromatic compound stubs
73:group. There are three
47:methoxybenzoyl chloride
128:This article about an
39:
93:—the location of the
26:of anisoyl chloride:
22:
188:Benzene derivatives
53:, specifically an
40:
24:Positional isomers
145:
144:
205:
166:
159:
152:
124:
117:
43:Anisoyl chloride
213:
212:
208:
207:
206:
204:
203:
202:
173:
172:
171:
170:
103:
67:carboxylic acid
61:by replacing a
17:
12:
11:
5:
211:
209:
201:
200:
195:
193:Acyl chlorides
190:
185:
175:
174:
169:
168:
161:
154:
146:
143:
142:
132:compound is a
125:
114:
113:
109:
102:
99:
15:
13:
10:
9:
6:
4:
3:
2:
210:
199:
198:Phenol ethers
196:
194:
191:
189:
186:
184:
181:
180:
178:
167:
162:
160:
155:
153:
148:
147:
141:
139:
135:
131:
126:
123:
119:
112:
110:
108:
105:
104:
100:
98:
96:
92:
88:
84:
80:
76:
72:
68:
65:group of the
64:
60:
56:
52:
48:
45:(also called
44:
37:
33:
29:
25:
21:
138:expanding it
127:
86:
82:
78:
46:
42:
41:
35:
31:
27:
59:anisic acid
51:acyl halide
177:Categories
101:References
130:aromatic
71:chloride
63:hydroxyl
55:aromatic
49:) is an
95:methoxy
75:isomers
69:with a
85:, and
79:ortho-
77:: the
87:para-
83:meta-
28:ortho
134:stub
36:para
32:meta
179::
81:,
165:e
158:t
151:v
140:.
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