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Detail of "6575-27-5"

  • CAS Number:
  • 6575-27-5
  • Name:

  • Benzenemethanamine,2,6-dichloro-

  • Superlist Name:
  • 2,6-Dichlorobenzylamine
  • Molecular Structure:
  • Formula:
  • C7H7Cl2N
  • Molecular Weight:
  • 176.04
  • Synonyms:
  • 2,6-Dichlorobenzylamine;Benzylamine,2,6-dichloro- (6CI,7CI,8CI);(2,6-Dichlorophenyl)methanamine;2,6-Dichlorobenzenemethanamine;
  • Density:
  • 1.32 g/cm3
  • Melting Point:
  • 40°C
  • Boiling Point:
  • 251.3 °C at 760 mmHg
  • Flash Point:
  • 105.8 °C
  • Appearance:
  • Clear pale yellow liquid
  • Hazard Symbols:
  • CorrosiveC
  • Risk Codes:
  • 34
  • Safety:
  • 45-36/37/39-26 Details
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CAS No.6575-27-5 2,6-Dichlorobenzylamine

Product Description Refined Naphthalene is the most important condensed-nuclei aromatics in industry. Its Molecular Formula is C10H8, Which is the coal tar's most abundant constituent, and usually it is produced by recycling from distilling coal tar and coke-oven gas or by

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CAS No.6575-27-5 2,6-Dichlorobenzylamine

2,6-Dichlorobenzylamine

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CAS No.6575-27-5 2,6-Dichlorobenzylamine

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CAS No.6575-27-5 2,6-Dichlorobenzylamine

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

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CAS No.6575-27-5 2,6-Dichlorobenzylamine

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CAS No.6575-27-5 2,6-Dichlorobenzylamine

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Supplier:Wako Pure Chemical Industries, Ltd. [ Japan]

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CAS No.6575-27-5 2,6-Dichlorobenzylamine

Molecular Formula:C7H7Cl2N Purity：98.0%

Supplier:Taizhou Medicine & Chemical Research Institute [ China (Mainland)]

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CAS No.6575-27-5 2,6-Dichlorobenzylamine

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CAS No.6575-27-5 2,6-Dichlorobenzylamine

Supplier:Chemosyntha NV [ Belgium]

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Reference

Dopamine b-hydroxylase inhibitors
Dopamine b-hydroxylase inhibitors. Kaiser, Carl; Kruse, Lawrence Ivan (SmithKline Beckman Corp., USA). Eur. Pat. Appl. EP 191621 A2 20 Aug 1986, 42 pp. DESIGNATED STATES: R: AT, BE, CH, DE, FR, GB, IT, LI, LU, NL, SE. (European Patent Organization) CODEN: EPXXDW. CLASS: ICM: C07D257-04. ICS: C07C161-04; C07C155-08; A61K031-41. APPLICATION: EP 86-300898 10 Feb 1986. PRIORITY: US 85-700234 11 Feb 1985. DOCUMENT TYPE: Patent CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Section cross-reference(s): 1, 63 (Phenalkyl)(mercapto)tetrazoles I (R = H, C1-4 alkyl; R1-R5 = H, halo, OH, C1-4 alkyl, cyano, NO2, SO2NH2, CO2H, CONH2, CHO, CH2OH, CF3, C1-4 alkoxy, etc.; n = 1-5), which inhibit dopamine b-hydroxylase, are prepd. Thus, 3,5-Cl2C6H3CHO was treated sequentially with MeONH2 and BH3-THF to give 3,5-Cl2C6H4CH2NH2, then with CS2 and MeI to give 3,5-Cl2C6H4CH2NHCS2Me. 90418-21-6 and 6575-27-5 which are cas registry numbers of chemicals are mentioned. The latter reacted with NaN3 to give mercaptotetrazole II. II was formulated as capsules contg. II 50, Mg stearate 5, and lactose 75 mg. II significantly decreased blood pressure in spontaneously hypertensive rats at 50 mg/kg i.p., and inhibited dopamine b-hydroxylase in vitro. .
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