Welcome to LookChem.com Sign In|Join Free

CAS

  • or

17264-54-9

Post Buying Request

17264-54-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

17264-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17264-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,6 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17264-54:
(7*1)+(6*7)+(5*2)+(4*6)+(3*4)+(2*5)+(1*4)=109
109 % 10 = 9
So 17264-54-9 is a valid CAS Registry Number.

17264-54-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,4-methylbenzoate

1.2 Other means of identification

Product number -
Other names sodium para-methylbenzoate

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:17264-54-9 SDS

17264-54-9Relevant articles and documents

Crystalline bis(η5-cyclopentadienyl)bis(benzoato/carboxylato)titanium(IV) precursor-directed route to functional titanium dioxide nanomaterials

Basu Baul, Tushar S.,Manne, Rajesh,Tiekink, Edward R. T.

, p. 3458 - 3475 (2018)

Five titanocene(IV) carboxylates of the general formula Cp2Ti(O2CR)2 viz., [Ti(η5-C5H5)2(O2CC6H5-4-CH3)2] (1), [Ti(η5

Kinetics and mechanism of alkaline hydrolysis of hydroxamic acids

Ghosh, Kallol K.,Thakur, Santosh S.

, p. 28 - 30 (2007/10/03)

Kinetics and mechanism of the alkaline hydrolysis of N-p-tolylbenzohydroxamic acid (p-X-C6H4(C=O)N(OH)C6H4-CH 3; X = H, CH3, Cl) and its para-substituted methyl and chloro derivatives have been studied in 10% (v/v) aqueous dioxane at 65°. Two cases of hydrolysis applicable to two different ranges of NaOH concentrations are recognized. The relative reactivity, temperature, salt, solvent and solvent isotope effects have also been examined.

Substituent Constants of the Pyrazol, 1,2,3-Triazol, Benzotriazol, and Naphthotriazol Group

Sachweh, Volker,Langhals, Heinz

, p. 1627 - 1639 (2007/10/02)

The synthesis of benzoic acids with the title substituents in p- and m-position (15, 13, 11, 9) and their ethyl and methyl esters is described.The ?p and ?m values of the substituents obtained by alkaline hydrolysis of the esters in ethanol/water and methylcellosolve/water demonstrate an inductive electron withdrawing and a mesomer electron donating effect of these groups which are important for dye chemistry.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 17264-54-9