Welcome to LookChem.com Sign In|Join Free

CAS

  • or
3-(1H-TETRAZOL-5-YL)BENZALDEHYDE is a chemical compound that features a benzene ring with a tetrazol-5-yl group and an aldehyde functional group. It is recognized for its role as a building block in the synthesis of pharmaceutical and agrochemical compounds, as well as serving as a chemical intermediate in organic synthesis. 3-(1H-TETRAZOL-5-YL)BENZALDEHYDE is also noted for its potential biological activity, making it a subject of interest in the pharmaceutical industry for its possible applications in medicine and material development.

136689-94-6 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 136689-94-6 Structure
  • Basic information

    1. Product Name: 3-(1H-TETRAZOL-5-YL)BENZALDEHYDE
    2. Synonyms: 3-(1H-TETRAZOL-5-YL)BENZALDEHYDE;3-(2H-Tetrazol-5-yl)benzaldehyde;3-(2H-1,2,3,4-tetrazol-5-yl)benzaldehyde
    3. CAS NO:136689-94-6
    4. Molecular Formula: C8H6N4O
    5. Molecular Weight: 174.15944
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 136689-94-6.mol
  • Chemical Properties

    1. Melting Point: 196-198 °C
    2. Boiling Point: 416.0±47.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.400±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. PKA: 3.99±0.10(Predicted)
    10. CAS DataBase Reference: 3-(1H-TETRAZOL-5-YL)BENZALDEHYDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(1H-TETRAZOL-5-YL)BENZALDEHYDE(136689-94-6)
    12. EPA Substance Registry System: 3-(1H-TETRAZOL-5-YL)BENZALDEHYDE(136689-94-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 136689-94-6(Hazardous Substances Data)

136689-94-6 Usage

Uses

Used in Pharmaceutical Industry:
3-(1H-TETRAZOL-5-YL)BENZALDEHYDE is used as a building block for the synthesis of various pharmaceutical compounds due to its unique chemical structure and potential biological activity, which can contribute to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 3-(1H-TETRAZOL-5-YL)BENZALDEHYDE is utilized as a key component in the creation of agrochemicals, leveraging its chemical properties to enhance crop protection and management products.
Used in Organic Synthesis:
3-(1H-TETRAZOL-5-YL)BENZALDEHYDE is used as a chemical intermediate in organic synthesis, facilitating the production of a range of organic compounds for various applications across different industries.
Used in Material Development:
3-(1H-TETRAZOL-5-YL)BENZALDEHYDE is also being investigated for its potential use in the development of new materials, capitalizing on its chemical properties to create innovative substances with unique characteristics.
Used as a Reagent in Organic Chemistry Reactions:
3-(1H-TETRAZOL-5-YL)BENZALDEHYDE serves as a reagent in various organic chemistry reactions, playing a crucial role in facilitating specific chemical transformations and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 136689-94-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,6,8 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 136689-94:
(8*1)+(7*3)+(6*6)+(5*6)+(4*8)+(3*9)+(2*9)+(1*4)=176
176 % 10 = 6
So 136689-94-6 is a valid CAS Registry Number.

136689-94-6SDS

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-(2H-tetrazol-5-yl)benzaldehyde

1.2 Other means of identification

Product number -
Other names -

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:136689-94-6 SDS

136689-94-6Downstream Products

136689-94-6Relevant articles and documents

Zinc hydroxyapatite - Catalyzed efficient synthesis of 5-substituted 1H-tetrazoles

Lakshmi Kantam,Balasubrahmanyam,Shiva Kumar

, p. 1809 - 1814 (2006)

Zinc hydroxyapatite (ZnHAP) is an effective heterogeneous catalyst for the (2 + 3)-cycloaddition of sodium azide with nitriles to afford 5-substituted 1H-tetrazoles in good yields. The catalyst is recovered and reused for several cycles with consistent ac

Microwave assisted synthesis of novel tetrazole/sulfonamide derivatives based on octahydroacridine, xanthene and chromene skeletons as inhibitors of the carbonic anhydrases isoforms I, II, IV and VII

Esirden, ?brahim,Tan?, Muhammet,Supuran, Claudiu T.,Kaya, Muharrem

, p. 86 - 89 (2017)

The synthesis of novel tetrazole/sulfonamide derivatives based on octahydroacridine, xanthene and chromene scaffold by using microwave (MW) assisted techniques is reported in this study. These synthesized hybrid compounds were assayed for the inhibition o

Facile, highly efficient and novel method for synthesis of 5-substituted 1H-tetrazoles catalysed by copper(I) chloride

Esirden, Ibrahim,Ba?ar, Erhan,Kaya, Muharrem

, p. 1231 - 1236 (2015)

The present study on tetrazole compounds, which have a wide area of application, proposes a new, simple and highly effective method. A series of 5-substituted 1H-tetrazoles were synthesised in DMF via the [3 + 2] cycloaddition reaction, in which different

One-pot synthesis of 5-substituted lH-tetrazoles from aryl bromides with potassium hexakis(cyano-κC)ferrate(4 -)(K4[Fe(CN)6]) as cyanide source

Zhu, Yizhong,Ren, Yiming,Cai, Chun

, p. 171 - 175 (2009)

A one-pot procedure for the synthesis of 5-substituted 1H-tetrazoles through the three-component reaction between an aryl bromide, potassium hexakis(cyano-κC)ferrate(4 - ) (K4[Fe(CN)6]) and NaN3 catalyzed by [Pd(OAc)2

Design, synthesis and evaluation of 1,3,6-trisubstituted-4-oxo-1,4-dihydroquinoline-2-carboxylic acid derivatives as ETA receptor selective antagonists using FRET assay

Khadtare, Nikhil,Stephani, Ralph,Korlipara, Vijaya

, p. 2281 - 2285 (2017/05/10)

The endothelin axis and in particular the two receptor subtypes, ETA and ETB, are under investigation for the treatment of various diseases such as pulmonary arterial hypertension, fibrosis, renal failure and cancer. Previous work in

Synthesis of 5-substituted-1H-tetrazole derivatives using monodisperse carbon black decorated Pt nanoparticles as heterogeneous nanocatalysts

Baskaya, Gaye,Esirden, Ibrahim,Erken, Esma,Sen, Fatih,Kaya, Muharrem

, p. 1992 - 1999 (2017/01/28)

A facile and highly efficient protocol for synthesis of new 5-substituted 1H-tetrazoles derivatives has been developed by the assistance of vulcan carbon decorated based on monodisperse platinum nanoparticles (Pt NPs@VC) as superior and recyclable heterog

Identification of a New Class of Selective Excitatory Amino Acid Transporter Subtype 1 (EAAT1) Inhibitors Followed by a Structure-Activity Relationship Study

Hansen, Stinne W.,Erichsen, Mette N.,Fu, Bingru,Bj?rn-Yoshimoto, Walden E.,Abrahamsen, Bjarke,Hansen, Jacob C.,Jensen, Anders A.,Bunch, Lennart

, p. 8757 - 8770 (2016/10/22)

Screening of a small compound library at the three excitatory amino acid transporter subtypes 1-3 (EAAT1-3) resulted in the identification of compound (Z)-4-chloro-3-(5-((3-(2-ethoxy-2-oxoethyl)-2,4-dioxothiazolidin-5-ylidene)methyl)furan-2-yl)benzoic aci

RETRACTED ARTICLE: A rapid and novel method for the synthesis of 5-substituted 1H-tetrazole catalyzed by exceptional reusable monodisperse Pt NPs@AC under the microwave irradiation

Erken, Esma,Esirden, Ibrahim,Kaya, Muharrem,Sen, Fatih

, p. 68558 - 68564 (2015/09/01)

A series of 5-substituted 1H-tetrazoles were synthesized in DMF by the [3 + 2] cycloaddition reaction under the effect of microwave irradiation (10-30 min, fixed mode, 90 °C, 140 W) in the presence of highly efficient superior catalyst. For this reaction,

RETRACTED ARTICLE: Monodisperse Pt NPs@rGO as highly efficient and reusable heterogeneous catalysts for the synthesis of 5-substituted 1H-tetrazole derivatives

Esirden, Ibrahim,Erken, Esma,Kaya, Muharrem,Sen, Fatih

, p. 4452 - 4457 (2015/09/01)

Monodisperse platinum nanoparticles supported on reduced graphene oxide (Pt NPs@rGO) are stable, isolable, bottleable, long-lived, highly efficient and exceptionally reusable heterogeneous catalysts for the synthesis of 5-substituted 1H-tetrazoles from so

Thiosemicarbazones of formyl benzoic acids as novel potent inhibitors of estrone sulfatase

Jütten, Peter,Schumann, Winfried,H?rtl, Albert,Dahse, Hans-Martin,Gr?fe, Udo

, p. 3661 - 3666 (2008/02/11)

Thiosemicarbazones of the microbial metabolite madurahydroxylactone, a polysubstituted benzo[a]-naphthacenequinone, have been previously reported by us as potent nonsteroidal inhibitors of the enzyme estrone sulfatase (cyclohexylthiosemicarbazone 1, ICsu

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 136689-94-6