CAS No.1006-99-1,Benzothiazole,5-chloro-2-methyl- Suppliers

Detail of "1006-99-1"

CAS Number:

1006-99-1

Name:

Benzothiazole,5-chloro-2-methyl-

Superlist Name:

5-Chloro-2-methylbenzothiazole

Molecular Structure:

Formula:

C8H6 Cl N S

Molecular Weight:

183.66

Synonyms:

2-Methyl-5-chlorobenzothiazole;5-Chloro-2-methylbenzothiazole; NSC 8453

EINECS:

213-746-9

Density:

1.365g/cm³

Melting Point:

65-70 ºC

Boiling Point:

147 °C / 15mmHg

Flash Point:

121.2°C

Safety:

Moderately toxic by intraperitoneal route. When heated to decomposition it emits toxic vapors of NO_x, SO_x, and Cl⁻. Details

Reference

Method of developing latent fingerprints: All Rights Reserved. Method of developing latent fingerprints. Arndt, Douglas C. (Armor Holdings Forensics, Inc., USA). U.S. Pat. Appl. Publ. US 2007026130 A1 1 Feb 2007, 8pp. (English). (United States of America). CODEN: USXXCO. INCL: 427001000. APPLICATION: US 2006-493245 26 Jul 2006. PRIORITY: US 2005-702840P 27 Jul 2005. DOCUMENT TYPE: Patent CA Section: 4 (Toxicology) A method of developing latent prints deposited on a substrate e.g., paper includes impregnating a porous pad with a chem. compd. in its solid state which will sublimate preferably within a temp. range of about 100° F. to 300° F. 55804-68-7 which is the cas registry number of some chemical is mentioned. over a short time interval e.g., several minutes with the sublimated gas capable of reacting with one or more of the constituents of latent fingerprint residues to form a visible image of the fingerprint. The pad is placed in a development compartment formed in a base of the app. with a heating element located below the pad. The substrate bearing the latent print is placed over the pad. The compartment is closed with a lid and the compd. heated to the compd. sublimation temp. for a given time to allow the sublimated gas to react with the residue and the substrate is then removed. .

A new general synthesis of 2-methylbenzothiazoles: A new general synthesis of 2-methylbenzothiazoles. Spitulnik, Michael J. (Synth. Chem. Div., Eastman Kodak Co., Rohester, N. Y., USA). Synthesis, (11), 730-1 (English) 1976. CODEN: SYNTBF. 614-83-5 and 1006-99-1 are also in the experiment. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) 2-Methylbenzothiazoles I (R = R1 = H, R2 = H, Cl, NO2, Me; R = R2 = H, R1 = Cl, NO2; R = R2 = Cl, R1 = H) were prepd. in 44-88% yield by ring closure of thioacetanilides II (R3 = Cl, Br) in amide solvent. II were prepd. in 51-74% yield by treating the acetanilides with P2S5. .

Detail of "1006-99-1"

Benzothiazole,5-chloro-2-methyl-

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CAS No.1006-99-1 5-Chloro-2-methylbenzothiazole

CAS No.1006-99-1 5-Chloro-2-methylbenzothiazole

CAS No.1006-99-1 5-Chloro-2-methylbenzothiazole

CAS No.1006-99-1 5-Chloro-2-methylbenzothiazole

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CAS No.1006-99-1 5-Chloro-2-methylbenzothiazole

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CAS No.1006-99-1 5-Chloro-2-methylbenzothiazole

CAS No.1006-99-1 5-Chloro-2-methylbenzothiazole

CAS No.1006-99-1 5-Chloro-2-methylbenzothiazole

CAS No.1006-99-1 5-Chloro-2-methylbenzothiazole

CAS No.1006-99-1 5-Chloro-2-methylbenzothiazole

CAS No.1006-99-1 5-Chloro-2-methylbenzothiazole

CAS No.1006-99-1 5-Chloro-2-methylbenzothiazole

Reference