123013-13-8

• 

• Basic information

  1. Product Name: 3-TERT-BUTYL-2-HYDROXY-5-METHOXYBENZALDEHYDE
  2. Synonyms: 3-TERT-BUTYL-2-HYDROXY-5-METHOXYBENZALDEHYDE
  3. CAS NO:123013-13-8
  4. Molecular Formula: C₁₂H₁₆O₃
  5. Molecular Weight: 208.25364
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 123013-13-8.mol
  9. Article Data: 13

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 3-TERT-BUTYL-2-HYDROXY-5-METHOXYBENZALDEHYDE(CAS DataBase Reference)
  10. NIST Chemistry Reference: 3-TERT-BUTYL-2-HYDROXY-5-METHOXYBENZALDEHYDE(123013-13-8)
  11. EPA Substance Registry System: 3-TERT-BUTYL-2-HYDROXY-5-METHOXYBENZALDEHYDE(123013-13-8)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 123013-13-8(Hazardous Substances Data)

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• SDS
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• Downstream Products
• Article

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• 3-TERT-BUTYL-2-HYDROXY-5-METHOXYBENZALDEHYDE

  Cas No: 123013-13-8

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• 3-TERT-BUTYL-2-HYDROXY-5-METHOXYBENZALDEHYDE

  Cas No: 123013-13-8

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123013-13-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123013-13-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,0,1 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 123013-13:
(8*1)+(7*2)+(6*3)+(5*0)+(4*1)+(3*3)+(2*1)+(1*3)=58
58 % 10 = 8
So 123013-13-8 is a valid CAS Registry Number.

123013-13-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name	3-tert-butyl-2-hydroxy-5-methoxybenzaldehyde

1.2 Other means of identification

Product number	-
Other names	5-MeO-3-(t-Bu)-salicylaldehyde

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:123013-13-8 SDS

123013-13-8Upstream product

• 121-00-6 3-tert-Butyl-4-hydroxyanisole 
• 100-97-0 hexamethylenetetramine 
• 50-00-0 formaldehyd 

123013-13-8Downstream Products

• 191720-27-1 (R,R)-2,2'-[(1,2-cyclohexanediyl)bis(nitrilomethylidyne)]bis[4-methoxy-6-(1,1-dimethylethyl)phenol] 
• 123013-07-0 3'-tert-butyl-2'-hydroxy-5'-methoxy-3-benzylidene-dl-camphor 
• 6291-15-2 3-tert-butyl-2-hydroxy-5-methoxybenzoic acid 
• 1186297-33-5 2-tert-butyl-4-methoxy-6-[(pyridin-2-ylmethylimino)methyl]phenol 
• 1186297-34-6 2-tert-butyl-4-methoxy-6-(quinolin-8-yliminomethyl)phenol 
• 1133339-74-8 2-tert-butyl-6-([(6-fluoro-quinolin-2-ylmethyl)-pyridin-2-ylmethylamino]-methyl)-4-methoxyphenol 
• 1207671-17-7 C₃₂H₄₂N₄O₄S₂ 
• 215033-57-1 C₆H₂OCH₃C(CH₃)3OHCHN(C₆H₅) 
• 1300737-95-4 (R,R)-N-(3,5-di-tert-butyl-salicylidene)-N'-(3-tert-butyl-5-methoxysalicylidene)-1,2-cyclohexanediamine 
• 1620152-17-1 C₃₂H₄₄N₂O₄ 

123013-13-8Relevant articles and documents

Catalytic performance and mechanism of Cu(II)-hydrazone complexes as models of galactose oxidase

Shi, Huatian,Yin, Yegao

, p. 446 - 450 (2014)

As simulants of galactose oxidase (GO), three mononuclear Cu(II) complexes with 1-((3-t-Bu,5-R1)-salicylidenehydrazono),2-((3-t-Bu,5-R2)- salicylidenehydrazono)-1,2-diphenylethane (H2LBu,Bu: R1 = R2 = t-butyl; H2LMeO,

Salen/salan metallic complexes as redox labels for electrochemical aptasensors

Ben Jrad, Amani,Kanso, Hussein,Raviglione, Delphine,Noguer, Thierry,Inguimbert, Nicolas,Calas-Blanchard, Carole

, p. 12821 - 12824 (2019)

This work presents the synthesis and characterization of salen/salan metal complexes for their future application as electrochemical labels in affinity sensors. Due to its stability and electrochemical properties, an oxovanadium salan complex was selected

Elaboration on the Electronics of Salen Manganese Nitrides: Investigations into Alkoxy-Substituted Ligand Scaffolds

Hein, Nicholas M.,Macneil, Gregory A.,Storr, Tim

, p. 16895 - 16905 (2021/11/18)

The ligand electronics of salen manganese nitride complexes directly influence the locus of oxidation and, thus, the reactivity of the resulting oxidized species. This work investigates the influence of tert-butoxy, isopropoxy, and methoxy substituents on

Unprecedented reductive cyclisation of salophen ligands to tetrahydroquinoxalines during metal complex formation

Dowsett, Mark R.,Lamb, Katie J.,North, Michael,Parker, Rachel R.,Whitwood, Adrian C.

supporting information, p. 4844 - 4847 (2020/05/13)

The synthesis of novel tetrahydroquinoxalines by a metal induced one-electron reductive cyclisation of salophen ligands was found to occur when a salophen ligand was treated with chromium(ii) chloride or decamethylcobaltocene.

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