Cas 19205-05-1,4-nitrobenzaldehyde (3-methyl-1,3-benzothiazol-2(3H)-ylidene)hydrazone

19205-05-1

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Basic information

Product Name: 4-nitrobenzaldehyde (3-methyl-1,3-benzothiazol-2(3H)-ylidene)hydrazone
Synonyms: 4-nitrobenzaldehyde (3-methyl-1,3-benzothiazol-2(3H)-ylidene)hydrazone
CAS NO:19205-05-1
Molecular Formula: C₁₅H₁₂N₄O₂S
Molecular Weight: 312.34638
EINECS: N/A
Product Categories: N/A
Mol File: 19205-05-1.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-nitrobenzaldehyde (3-methyl-1,3-benzothiazol-2(3H)-ylidene)hydrazone(CAS DataBase Reference)
NIST Chemistry Reference: 4-nitrobenzaldehyde (3-methyl-1,3-benzothiazol-2(3H)-ylidene)hydrazone(19205-05-1)
EPA Substance Registry System: 4-nitrobenzaldehyde (3-methyl-1,3-benzothiazol-2(3H)-ylidene)hydrazone(19205-05-1)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 19205-05-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 19205-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,0 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19205-05:
(7*1)+(6*9)+(5*2)+(4*0)+(3*5)+(2*0)+(1*5)=91
91 % 10 = 1
So 19205-05-1 is a valid CAS Registry Number.

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19205-05-1Downstream Products

19205-05-1Relevant academic research and scientific papers

Synthesis and antitumor evaluation of new heterocycles derived from 3-Methyl-2-benzothiazolinone Hydrazone

Ibrahim, Nabila M.,Yosef, Hisham A.A.,Ewies, Ewies F.,Mahran, Mohamed R.H.,Ali, Mamdouh M.,Mahmoud, Abeer E.

, p. 1086 - 1097 (2015/06/16)

3-Methyl-2-benzothiazolinone hydrazone condensed with some selected aldehydes to give the corresponding Schiff bases. Cyclizing the obtained Schiff base derivatives with thioglycolic acid afforded the respective thiazolylideneaminothiazolidenones. Condens

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