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N-BENZYL-4,5,6,7-TETRAHYDRO-1,3-BENZOTHIAZOL-2-AMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15087-99-7

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15087-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15087-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,8 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15087-99:
(7*1)+(6*5)+(5*0)+(4*8)+(3*7)+(2*9)+(1*9)=117
117 % 10 = 7
So 15087-99-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H16N2S/c1-2-6-11(7-3-1)10-15-14-16-12-8-4-5-9-13(12)17-14/h1-3,6-7H,4-5,8-10H2,(H,15,16)

15087-99-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-4,5,6,7-tetrahydro-1,3-benzothiazol-2-amine

1.2 Other means of identification

Product number -
Other names 2-Benzylamino-4,5,6,7-tetrahydro-benzothiazole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15087-99-7 SDS

15087-99-7Downstream Products

15087-99-7Relevant academic research and scientific papers

Condensed Tetrahydrobenzothiazoles: Part IV - Synthesis of Some 2-Substituted 4,5,6,7-Tetrahydrobenzothiazoles and Their 5,5 Dimethyl-7-oxo Derivatives

Udapudi, V. T.,Mahajanshetti, C. S.

, p. 1269 - 1272 (2007/10/02)

Condensation of 2-chlorocyclohexanone (I) with substituted thioamides (II) in hot ethanol affords 2-substituted 4,5,6,7-tetrahydrobenzothiazoles (III).A similar reaction of 2-bromodimedone (IV) with II does not give 2-substituted 5,5-dimethyl-7-oxo-4,5,6,7-tetrahydrobenzothiazoles alone (V); a gummy product containing more than two compounds (TLC) is obtained in each case.However, When the reaction is carried out in THF at room temperature for 36 hr, the expected hydrobromide salts (Va) are obtained in excellent yields.The free bases (V) are liberated from Va by treatment with Na2CO3 solution.Structures of III, Va and V have been established by elemental analyses and spectral data.They do not exhibit any significant antifungal or antibacterial activity in vitro.

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