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2-Amino-4-methylanisole

Name: 2-Amino-4-methylanisole

CA Name: Benzenamine,2-methoxy-5-methyl-

Molecular Structure:

2-Amino-4-methylanisole,Benzenamine,2-methoxy-5-methyl-,CAS 120-71-8,137.18,C8H11NO

2-Amino-4-methylanisole,Benzenamine,2-methoxy-5-methyl-,CAS 120-71-8,137.18,C8H11NO

Molecular Formula:C8H11NO

Molecular Weight: 137.18

CAS Registry Number: 120-71-8

List of synthetic dyes :

C.I.Azoic Diazo Component 39

C.I.Azoic Diazo Component 41

C.I.Disperse Orange 121

C.I.Disperse Orange 20

C.I.Disperse Orange 21

C.I.Disperse Orange 38

C.I.Disperse Black 2

C.I.Disperse Red 31

C.I.Reactive Yellow 84

C.I.Basic Orange 29

C.I.Basic Yellow 62

C.I.Mordant Red 80

C.I.Solvent red 17

C.I.Solvent Yellow 134

C.I.Acid Orange 128

C.I.Acid Orange 156

C.I.Acid Black 4

C.I.Acid Red 21

C.I.Acid Red 21

C.I.Acid Violet 131

C.I.Direct Orange 37

C.I.Direct Orange 40

C.I.Direct Orange 49

C.I.Direct Orange 62

C.I.Direct Orange 69

C.I.Direct Orange 72

C.I.Direct Orange 83

C.I.Direct Black 1

C.I.Direct Black 17

C.I.Direct Black 96

C.I.Direct Red 187

C.I.Direct Red 76

C.I.Direct Red 79

C.I.Direct Red 89

C.I.Direct Yellow 134

C.I.Direct Yellow 138

C.I.Direct Yellow 167

C.I.Direct Yellow 34

C.I.Direct Yellow 41

C.I.Direct Yellow 42

C.I.Direct Yellow 67

C.I.Direct Yellow 79

C.I.Direct Yellow 83

C.I.Direct Blue 111

C.I.Direct Blue 116

C.I.Direct Blue 124

C.I.Direct Blue 126

C.I.Direct Blue 128

C.I.Direct Blue 145

C.I.Direct Blue 162

C.I.Direct Blue 163

C.I.Direct Green 26

C.I.Direct Violet 31

C.I.Direct Violet 51

C.I.Direct Violet 9

C.I.Direct Blue 29

C.I.Direct Green 59

C.I.Direct Violet 35

C.I.Direct Violet 64

C.I.Direct Brown 126

C.I.Direct Blue 67

C.I.Direct Violet 11

C.I.Direct Violet 40

C.I.Direct Violet 72

C.I.Direct Brown 99


10 Responses to “2-Amino-4-methylanisole”

  1. […] mol) and 2,4,6-Trichloro-1,3,5-triazine(2 moles) and 2-Amino-4-methylanisole(2 moles) condensation, and then with diazotized 7-Aminonaphthalene-1,3-disulfonic acid […]

  2. […] Methods : 3-Aminobenzenesulfonic acid diazo, and 2-Amino-4-methylanisole coupling, and then will light product for […]

  3. […] Methods : 7-Aminonaphthalene-1,3-disulfonic acid diazo, and 2-Amino-4-methylanisole coupling, and then make the light […]

  4. […] Methods : 1-Amino-2-naphthalene sulfonic acid diazo, and 2-Amino-4-methylanisole coupling, its product to diazo, in alkaline conditions and […]

  5. […] Methods : 5-Amino-8-nitronaphthalene-2-sulfonic acid diazo, and 2-Amino-4-methylanisole coupling, again diazotization and 7-Hydroxynaphthalene-2-sulfonic acid coupling, and then will the […]

  6. […] Methods : 4-Aminobenzenesulfonic acid diazo, and 2-Amino-4-methylanisole coupled to compounds (A); 4-Nitrobenzenamine diazo, coupled with 2-Hydroxybenzoic acid, and then […]

  7. […] Methods : 5-Amino-2-chlorobenzenesulfonic acid diazo, and 2-Amino-4-methylanisole coupled to compounds (A); 4-Nitrobenzenamine diazo, coupled with 2-Hydroxybenzoic acid, and then […]

  8. […] Methods : 5-Amino-2-methoxybenzenesulfottic acid diazo, and 2-Amino-4-methylanisole coupling, compounds (A); 4-Nitrobenzenamine diazo, coupled with 2-Hydroxybenzoic acid, and then […]

  9. […] Methods :  5-Amino-2-hydroxybenzoic acid diazo, and 2-Amino-4-methylanisole coupling, its product (2 Moore) diazo, and Bis(4-hydroxy-2-sulfonaphthalene-7-yl)amine […]

  10. […] Methods : 2-Hydroxy-3-nitro-5-aminobenzenesulfonic acid diazotization, and 2-Amino-4-methylanisole coupling, product to diazotization, and 2-Hydroxy-3-methylbenzoic acid […]

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