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73900-07-9

METHYL-D3 TRIFLATE is a deuterated analog of the powerful methylating agent, methyl triflate, commonly used in synthetic preparations of organic compounds.

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  • 73900-07-9 Structure

  • Basic information

    1. Product Name: METHYL-D3 TRIFLATE
    2. Synonyms: METHYL-D3 TRIFLATE;METHYL-D3 TRIFLUOROMETHANESULFONATE;OIRDBPQYVWXNSJ-FIBGUPNXSA-N
    3. CAS NO:73900-07-9
    4. Molecular Formula: C2H3F3O3S
    5. Molecular Weight: 167.12
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 73900-07-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 94-99 °C(lit.)
    3. Flash Point: 101 °F
    4. Appearance: /
    5. Density: 1.477 g/mL at 25 °C(lit.)
    6. Refractive Index: n20/D 1.325(lit.)
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: METHYL-D3 TRIFLATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: METHYL-D3 TRIFLATE(73900-07-9)
    11. EPA Substance Registry System: METHYL-D3 TRIFLATE(73900-07-9)

  • Safety Data

    1. Hazard Codes: T
    2. Statements: 10-23/24/25-34-40
    3. Safety Statements: 16-26-36/37/39-45
    4. RIDADR: UN 2920 8/PG 2
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 73900-07-9(Hazardous Substances Data)

73900-07-9 Usage

Uses

Used in Organic Synthesis:
METHYL-D3 TRIFLATE is used as a methylating reagent for the synthesis of various organic compounds, providing a stable and efficient method for introducing deuterium-labeled methyl groups into target molecules. This is particularly useful in the study of reaction mechanisms, structural elucidation, and the development of new synthetic routes.

Check Digit Verification of cas no

The CAS Registry Mumber 73900-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,0 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73900-07:
(7*7)+(6*3)+(5*9)+(4*0)+(3*0)+(2*0)+(1*7)=119
119 % 10 = 9
So 73900-07-9 is a valid CAS Registry Number.

73900-07-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name trideuteriomethyl trifluoromethanesulfonate

1.2 Other means of identification

Product number -
Other names Methyl-d3 triflate

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:73900-07-9 SDS

73900-07-9Relevant articles and documents

Robust, scalable construction of an electrophilic deuterated methylthiolating reagent: facile access to SCD3-containing scaffolds

Bai, Jun,Chen, Fen-Er,Cheng, Fei,Huang, Yin-Qiu,Ke, Miao-Lin,Tian, Hong-Yu,Wang, Xu,Xiao, Xiao

supporting information, p. 3015 - 3018 (2022/03/14)

We have established a practical and concise method for the straightforward access of a universal deuterated methylthiolating reagent through a one-pot gram-scale operation under mild conditions. This odourless electrophilic SCD3 reagent was widely applied to react with numerous representative nucleophiles and approached various valuable SCD3 analogues with excellent levels of deuterium content (>99% D). The divergent further transformations were smoothly carried out to obtain the significant derivatives with different oxidative states in high efficiency.

Reactivity in Methyl Transfer Reactions. 5. Relation between Rates and Equilibria

Lewis, Edward S.,Kukes, Semyon,Slater, Carl D.

, p. 1619 - 1623 (2007/10/02)

The methyl transfer reactions of two dimethylarylsulfonium ions with methyl phenyl sulfide are equilibrated in sulfolane solutions, as is the methyl transfer from methyldiphenylsulfonium ion to methyl 3,4-dichlorophenyl sulfide, and from dimethyl sulfate

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