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67130-14-7

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67130-14-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67130-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,1,3 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67130-14:
(7*6)+(6*7)+(5*1)+(4*3)+(3*0)+(2*1)+(1*4)=107
107 % 10 = 7
So 67130-14-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H16N2/c1-5-6(2)8(4)10(12)9(11)7(5)3/h11-12H2,1-4H3

67130-14-7SDS

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 3,4,5,6-tetramethylbenzene-1,2-diamine

1.2 Other means of identification

Product number -
Other names 3,4,5,6-Tetramethylbenzol-1,2-diamin

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:67130-14-7 SDS

67130-14-7Relevant articles and documents

Synthesis and activity of 1H-benzimidazole and 1H-benzotriazole derivatives as inhibitors of Acanthamoeba castellanii

Kopańska, Katarzyna,Najda, Andzelika,Zebrowska, Justyna,Chomicz, Lidia,Piekarczyk, Janusz,Myjak, Przemys?aw,Bretner, Maria

, p. 2617 - 2624 (2007/10/03)

Chloro-, bromo- and methyl- analogues of 1H-benzimidazole and 1H-benzotriazole and their N-alkyl derivatives have been synthesized and tested in vitro against the protozoa Acanthamoeba castellanii. The results indicate that 5,6-dimethyl-1H-benzotriazole (11) and 5,6-dibromo-1H-benzotriazole (14) have higher efficacy than the antiprotozoal agent chlorohexidine.

A NEW SYNTHESIS OF DIAMINOPREHNITOL

D'yachenko, E. K.,Pesin, V. G.,Papirnik, M. P.

, p. 372 - 375 (2007/10/02)

The reaction of 4,7-di(chloromethyl)-5,6-dimethylbenzo-2,1,3-thiadiazole with a small excess of tin(II) chloride leads to a high yield of tetramethylbenzo-2,1,3-thiadiazole.With a large excess of tin chloride the thiadiazole ring is cleaved to 1,2,3,4-tet

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