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Detail of "55067-10-2"

  • CAS Number:
  • 55067-10-2
  • Name:
  • Cyanamide,N-(1,4,5,6-tetrahydro-4,6-dioxo-2-pyrimidinyl)-

  • Superlist Name:
  • 2-Cyanoamino-4,6-dihydroxypyrimidine
  • Molecular Structure:
  • Formula:
  • C5H4N4O2
  • Molecular Weight:
  • 152.11
  • Synonyms:
  • 2-Pyrimidinecarbamonitrile,4,6-dihydroxy- (7CI);Cyanamide, (1,4,5,6-tetrahydro-4,6-dioxo-2-pyrimidinyl)-(9CI);Cyanoiminobarbituric acid;2-Cyanoamino-4,6-dihydroxypyrimidine;
  • EINECS:
  • 259-467-6
  • Density:
  • 1.69 g/cm3

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CAS No.55067-10-2 2-Cyanoamino-4,6-dihydroxypyrimidine

Stardard:98% Package: 25KG/plastics drum

Supplier:Jiangsu Taicang Qianjing Chemical Co., Ltd. [ China (Mainland)]

Manufacturer 813Integral
813

Tel:86)-512-53648666

Address:9 Dongfang Road, Gangkou Development Zone, taicang, Jiangsu China

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CAS No.55067-10-2 2-Cyanoamino-4,6-dihydroxypyrimidine

Supplier:Shijiazhuang JuSha Imp. & Exp. Co., Ltd [ China (Mainland)]

Platinum
Supplier
910Integral
910

Tel:86-311-89877166

Address:Room 307, XinCheng Building, No. 351 YouYi Street, Shijiazhuang, China

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CAS No.55067-10-2 2-Cyanoamino-4,6-dihydroxypyrimidine

2-Cyanoiminobarbituric acid

Supplier:Wide Rao Juze Chemical Co., Ltd. [ China (Mainland)]

266Integral
266

Tel:0533-2865566

Address:3 Toranomon Denki building 2-8-1, Toranomon, Minato-ku, Tokyo

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CAS No.55067-10-2 2-Cyanoamino-4,6-dihydroxypyrimidine

Supplier:JUZEN CHEMICAL CORPORATION [ Japan]

10Integral
10

Tel:+81-76-433-1111

Address:1-10, Kiba-machi, Toyama, Japan

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Reference

Pyrimidine azo pigments
Pyrimidine azo pigments. Lorenz, Manfred; Schuendehuette, Karl Heinz; Bornatsch, Wolfgang (Bayer A.-G. , Fed. Rep. Ger.). Ger. Offen. DE 3307508 A1 3 Nov 1983, 48 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C09B029-036; C09B041-00. APPLICATION: DE 83-3307508 3 Mar 1983. PRIORITY: DE 82-3215877 29 Apr 1982. DOCUMENT TYPE: Patent CA Section: 41 (Dyes, Organic Pigments, Fluorescent Brighteners, and Photographic Sensitizers) The title azo compds. RN:NR1 (I; R 1 R1, R = R2 or R3 or their tautomers and R1 = coupling component residue) were prepd. by coupling R1H with II or III, prepd. by resp. reaction of R2H or R3H with Z(SO2N3)n [where Z = alkyl or aryl residue, n = 1-3, R4, R6 = O, N(CN), or substituted imino, and R5, R7 = H, heterocyclic residue, optionally substituted alkyl, cycloalkyl, aryl, aralkyl, or amino].In this experiment, several chemicals are used like 86264-28-0 and 88638-15-7 Thus, benzenesulfonyl hydrazide [80-17-1] was treated with HNO2 to give an emulsion of benzenesulfonyl azide [938-10-3], and barbituric acid [67-52-7] was added to the mixt. to give a suspension of Na diazobarbiturate [88638-09-9]. To this suspension 2-cyaniminobarbituric acid [55067-10-2] was added to give Na monocyaniminobarbiturate [88638-10-2] and the suspension was acidified to pH 1 with HCl and heated at 95° to give (IV) [86248-19-3], coloring lacquer and plaster in clear orange shades. .
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