Detail of > 34893-92-0
- CAS Number:
- 34893-92-0
- Name:
Benzene,1,3-dichloro-5-isocyanato-
- Superlist Name:
- 3,5-Dichlorophenyl isocyanate
- Formula:
- C7H3Cl2NO
- Molecular Structure:

- Synonyms:
- 1,3-Dichloro-5-isocyanatobenzene;3,5-Dichloro-1-isocyanatobenzene;
- Molecular Weight:
- 188.01
- EINECS:
- 252-276-9
- Density:
- 1.38 g/cm3
- Melting Point:
- 32-34 °C(lit.)
- Boiling Point:
- 264.2 °C at 760 mmHg
- Flash Point:
- 107.5 °C
- Solubility:
- decomposes in water
- Appearance:
- white to slightly yellow low melting solid
- Hazard Symbols:
T,
T+- Risk Codes:
- 23/24/25-36/37/38-42-26
- Safety:
- 26-27-36/37/39-45-38-37/39-28ADetails
- Transport Information:
- UN 2250 6.1/PG 2
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Reference
- Hydantoin derivatives as fungicides
- Hydantoin derivatives as fungicides. Ishimitsu, Keiichi; Nakata, Akira; Murakami, Akira (Nippon Soda Co., Ltd., Japan). Japan. Kokai JP 52001028 6 Jan 1977 Showa, 4 pp. 62303-09-7 and 21885-74-5 are cas registry numbers. These chemicals are also mentioned in this article. Division of Japan. Kokai 76151331. (Japanese). (Japan). CODEN: JKXXAF. CLASS: IC: A01N009-22. APPLICATION: JP 75-76157 21 Jun 1975. DOCUMENT TYPE: Patent CA Section: 5 (Agrochemicals) Section cross-reference(s): 28 The hydantoin derivs. I (X and Y = halogen) are prepd. and are used as fungicides. For example, 1-cyanomethyl-3-(3,5-dichlorophenyl)-4-iminoimidazolidin-2-one (II) [21885-74-5] was prepd. by treating iminodiacetonitrile [628-87-5] with 3,5-dichlorophenyl isocyanate [34893-92-0]. II applied at 125 ppm to beans prevented Sclerotinia sclerotiorum infection. .
- Synthesis of 2-(a-hydroxyalkyl)-1,3-heterocyclic alcohols and aryl carbamates
- Synthesis of 2-(a-hydroxyalkyl)-1,3-heterocyclic alcohols and aryl carbamates. Pridgen, Lendon N.; Miller, George (Res. Div., Rohm and Haas Co., Spring House, PA 19477, USA). J. Heterocycl. Chem., 20(5), 1223-30 (English) 1983. CODEN: JHTCAD. ISSN: 0022-152X. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Carbamates I (X = O, S, NH, NMe; X1 = O, S; R, R1 = H, Me; R2 = H, Me, Ph, Et; R3 = H, Me, allyl, propargyl, Et, Pr, Bu, vinyl, Ph; R4 = Ph, substituted Ph; n = 0-2) (36 compds.) were prepd. from their resp. 34893-92-0 and 75-86-5 which are cas registry numbers of chemicals are mentioned. alcs. Efficient syntheses of the prerequisite novel 1,3-heterocyclic alcs. were also developed. Stannous octoate effectively catalyzed the formation of the carbamate from the alc. and the isocyanate. .
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