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CAS

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134839-87-5

D3-METHYL BENZOYLFORMATE is a white, crystalline chemical compound belonging to the class of organic compounds known as benzoylformates. It is characterized by its sweet, fruity aroma and is commonly used in various industries due to its distinctive scent.

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  • 134839-87-5 Structure

  • Basic information

    1. Product Name: D3-METHYL BENZOYLFORMATE
    2. Synonyms: METHYL-D3 PHENYLGLYOXYLATE;D3-METHYL BENZOYLFORMATE
    3. CAS NO:134839-87-5
    4. Molecular Formula: C9H8O3
    5. Molecular Weight: 167.18
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134839-87-5.mol

  • 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: D3-METHYL BENZOYLFORMATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: D3-METHYL BENZOYLFORMATE(134839-87-5)
    11. EPA Substance Registry System: D3-METHYL BENZOYLFORMATE(134839-87-5)

  • 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: 134839-87-5(Hazardous Substances Data)

134839-87-5 Usage

Uses

Used in Food Industry:
D3-METHYL BENZOYLFORMATE is used as a flavoring agent for its sweet, fruity aroma, enhancing the taste and smell of various food products.
Used in Perfume and Fragrance Industry:
D3-METHYL BENZOYLFORMATE is used as a key ingredient in the production of perfumes and other fragrances, providing a pleasant and attractive scent.
Used in Pharmaceutical Industry:
D3-METHYL BENZOYLFORMATE is utilized in the synthesis of pharmaceuticals and other organic compounds, contributing to the development of new medications and treatments.
Used in Chemical Synthesis:
D3-METHYL BENZOYLFORMATE is used as a reagent in the synthesis of various organic compounds, playing a crucial role in chemical research and development.
Note: Due to its potential for skin and eye irritation, D3-METHYL BENZOYLFORMATE should be handled and used with care to ensure safety.

Check Digit Verification of cas no

The CAS Registry Mumber 134839-87-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,3 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 134839-87:
(8*1)+(7*3)+(6*4)+(5*8)+(4*3)+(3*9)+(2*8)+(1*7)=155
155 % 10 = 5
So 134839-87-5 is a valid CAS Registry Number.

134839-87-5SDS

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 D3-METHYL BENZOYLFORMATE

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:134839-87-5 SDS

134839-87-5Relevant articles and documents

Synthesis and Properties of 1-Acyl Triazenes

Landman, Iris R.,Acu?a-Bolomey, Emilio,Scopelliti, Rosario,Fadaei-Tirani, Farzaneh,Severin, Kay

, p. 6408 - 6412 (2019/09/06)

1-Acyl triazenes can be prepared by acid-catalyzed hydration, gold/iodine-catalyzed oxidation, or oxyhalogenation of 1-alkynyl triazenes. Crystallographic analyses reveal a pronounced effect of the acyl group on the electronic structure of the triazene fu

An efficient and practical synthesis of aryl and hetaryl α-keto esters

Raghunadh, Akula,Meruva, Suresh Babu,Kumar, Nuka Anil,Kumar, Gudla Santosh,Rao, L. Vaikunta,Syamkumar

supporting information; experimental part, p. 283 - 289 (2012/03/26)

A general and highly efficient method was developed for the synthesis of -keto esters by oxidative esterification of 2,2-dibromo-1-(het)arylethanones by sequential treatment with dimethyl sulfoxide and an alkanol. The versatility of the reaction was established by synthesizing a range of -keto esters by treatment of 2,2-dibromoethanones, derived from aryl or hetaryl ketones, with di-methyl sulfoxide and a cyclic or acyclic primary or secondary alcohol. The mechanism of the reaction was established by means of a detailed study. Georg Thieme Verlag Stuttgart · New York.

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