Detail of "95-79-4"

CAS Number:
95-79-4
Name:
Benzenamine,5-chloro-2-methyl-
Superlist Name:
5-Chloro-2-methylaniline
Molecular Structure:
Formula:
C₇H₈ClN
Molecular Weight:
141.61
Synonyms:
Fast Red KBBase (6CI);o-Toluidine, 5-chloro- (8CI);2-Amino-4-chlorotoluene;2-Methyl-5-chloroaniline;3-Chloro-6-methylaniline;4-Chloro-2-aminotoluene;5-Chloro-2-methylaniline;5-Chloro-2-methylbenzenamine;5-Chloro-2-methylphenylamine;5-Chloro-2-toluidine;5-Chloro-o-toluidine;AccoFast Red KB base;Ansibase Red KB;Azoene Fast Red KB base;Fast Red KB amine;Fast Red KB salt;Fast Red KB salt Supra;Fast Red KB-T Base;Fast Red KBSsalt;Genazo Red KB soln;Hiltonil Fast Red KB base;Metrogen Red Former KBsoln;NSC 7094;Naphthosol Fast Red KB base;Pharmazoid Red KB;Red KB base;Spectrolene Red KB;Stable Red KB base;
EINECS:
202-452-6
Density:
1.18 g/cm³
Melting Point:
22 °C
Boiling Point:
237 °C at 760 mmHg
Flash Point:
160 °C
Solubility:
< 1 g/L (22 °C) in water
Appearance:
clear yellow to light brown liquid after melting
Hazard Symbols:
Xn, T
Risk Codes:
22-36/37/38-40-45-23/24/25
Safety:
26-45-36/37/39-53 Details
Transport Information:
UN 3429 6.1/PG 3

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CAS No.95-79-4 5-Chloro-2-methylaniline

Supplier:Changzhou Ansciep Chemical Co.,Ltd. [ China (Mainland)]

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CAS No.95-79-4 5-Chloro-2-methylaniline

Assay:99.5% Appearance:powder Package:25kg/Cardboa...Storage:1-10MT

Supplier:Henan Tianfu Chemical Co., Ltd. [ China (Mainland)]

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Assay:98%

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2-Amino-4-Chloro-Toluene

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5-Chloro-2-methylaniline

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CAS No.95-79-4 5-Chloro-2-methylaniline

5-Chloro-2-methyl aniline 1.Molecular formula: C7H8NCL 2.Structural formula: 3.Quality Index Item Index Synonyms 5-chlorine-o-toluidine; 2-amino-4-chlorotoluene Appearance light to red brown liquid Purity(%) >99% 3-Chloro-2-methyl aniline(%) <0.5 o-toluidine <0.5

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5-chloro-2-methyl aniline

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CAS No.95-79-4 5-Chloro-2-methylaniline

Molecular Formula: C7H8ClN Formula Weight: 141.6

Supplier:The Wujiang City Temple chemical plant [ China (Mainland)]

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Reference

Synthesis of dyes from 2-chloro-5-methyl-1,4-phenylenediamine: Synthesis of dyes from 2-chloro-5-methyl-1,4-phenylenediamine. Sebe, Ion; Popescu, Ioan Dan; Ganea, Adriana; Calota, Ioana (Inst. Politeh., Bucharest, Rom.). Ind. Usoara: Text., Tricotaje, Confectii Text., 35(8), 368-71 (Romanian) 1984. CODEN: IUSAAE. DOCUMENT TYPE: Journal CA Section: 41 (Dyes, Organic Pigments, Fluorescent Brighteners, and Photographic Sensitizers) Section cross-reference(s): 40 Reaction of the title compd. (I) [5307-03-9] with bromaminic acid Na salt [6258-06-6] gave II(R1 = SO3Na, R2 = NH2)(III) [96384-10-0], and redn. of III with glucose gave II(R1 = H, R2 = NH2)(IV) [96384-11-1], which was chloroacetylated to form II(R1 = H, R2 = NHCOCH2Cl)(V) [96384-12-2] and then quaternized with C5H5N and ZnCl2 to give II(R1 = H, R2 = NHCOCH2NC5H5.ZnCl3)(VI) [96384-14-4]. III colored wool dark blue; IV colored polyester fibers light blue-violet; V colored polyester fibers violet; and VI colored acrylic fibers violet. All the dyeings exhibited excellent light resistance and good resistance to rubbing and heat. I was prepd. by a series of reactions involving nitrating p-toluidine (VII) [106-49-0], diazotizing nitrated VII, conducting a Sandmeyer reaction on the resulting diazonium salt to give 4-chloro-2-nitrotoluene (VIII) [89-59-8], reducing VIII to 2-amino-4-chlorotoluene (IX) [95-79-4], acetylating IX to 5-chloro-2-methylacetanilide (X) [5900-55-0], nitrating X to 2-acetylamino-4-chloro-5-nitrotoluene [13852-50-1] (plus the 3-nitro isomer), hydrolyzing the isomer mixt., sepg. 2-amino-4-chloro-5-nitrotoluene (XI) [13852-51-2], and reducing XI.

Azo pigments, derivatives of quinoxaline: Azo pigments, derivatives of quinoxaline. Gerlicz, Anna; Kraska, Jan; Wojciechowski, Lech (Osrodek Badawczo-Rozwojowy Przemyslu Barwnikow, Pol.). Pol. PL 83414 15 Oct 1976, 2 pp. (Polish). (Poland). CODEN: POXXA7. CLASS: IC: C09B033-12. APPLICATION: PL 72-154436 31 Mar 1972. DOCUMENT TYPE: Patent CA Section: 40 (Dyes, Fluorescent Whitening Agents, and Photosensitizers) Azo pigments (I, R = H, Cl; R1 = H, NO2, NH2, acylamino; R2 = Ph, substituted Ph; Z = direct bond, O, S) are prepd. by coupling the corresponding bis(4-acetoacetamidophenyl) quinoxaline with diazotized R2NH2. Thus, 2,3-bis(4-acetoacetamidophenyl)quinoxaline [64084-29-3] is coupled with diazotized 2,5-MeClC6H3NH2 [95-79-4] to give yellow I(R = R1 = H, R2 = 2,5-MeClC6H3, Z = direct bond) [64084-30-6].

Detail of "95-79-4"

Benzenamine,5-chloro-2-methyl-

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CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

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CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

CAS No.95-79-4 5-Chloro-2-methylaniline

Reference