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CAS

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218628-86-5

1H-Thieno[3,4-c]pyrrole-4-carboxylic acid, 3,5-dihydro-, phenylmethyl ester, 2,2-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1H-Thieno[3,4-c]pyrrole-4-carboxylic acid, 3,5-dihydro-, phenylmethyl ester, 2,2-dioxide

    Cas No: 218628-86-5

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  • 218628-86-5 Structure

  • Basic information

    1. Product Name: 1H-Thieno[3,4-c]pyrrole-4-carboxylic acid, 3,5-dihydro-, phenylmethyl ester, 2,2-dioxide
    2. Synonyms:
    3. CAS NO:218628-86-5
    4. Molecular Formula: C14H13NO4S
    5. Molecular Weight: 291.328
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 218628-86-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1H-Thieno[3,4-c]pyrrole-4-carboxylic acid, 3,5-dihydro-, phenylmethyl ester, 2,2-dioxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Thieno[3,4-c]pyrrole-4-carboxylic acid, 3,5-dihydro-, phenylmethyl ester, 2,2-dioxide(218628-86-5)
    11. EPA Substance Registry System: 1H-Thieno[3,4-c]pyrrole-4-carboxylic acid, 3,5-dihydro-, phenylmethyl ester, 2,2-dioxide(218628-86-5)

  • 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: 218628-86-5(Hazardous Substances Data)

218628-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 218628-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,8,6,2 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 218628-86:
(8*2)+(7*1)+(6*8)+(5*6)+(4*2)+(3*8)+(2*8)+(1*6)=155
155 % 10 = 5
So 218628-86-5 is a valid CAS Registry Number.

218628-86-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-Dihydro-1H-thieno[3,4-c]pyrrolcarbonsaeure-benzylester

1.2 Other means of identification

Product number -
Other names benzyl pyrrole-2-carboxylate

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:218628-86-5 SDS

218628-86-5Relevant articles and documents

Symmetrical tetra-β″-sulfoleno-meso-aryl-porphyrins-synthesis, spectroscopy and structural characterization

Banala, Srinivas,Wurst, Klaus,Kr?utler, Bernhard

, p. 115 - 122 (2014/04/03)

We report here the preparation (in one-pot) of a tetra-β″- sulfoleno-meso-aryl-porphyrin in about 80% yield by using an optimized modification of Lindsey's variant of the Adler-Longo approach. The Zn(II)-, Cu(II)- and Ni(II)-complexes of the symmetrical p

Porphodimethylidenes from porphyrin-fused 3-sulfolenes - Versatile porphyrin dienes for cycloadditions

Gunter, Maxwell J.,Tang, Hesheng,Warrener, Ronald N.

, p. 803 - 804 (2007/10/03)

A porphyrin with a β-fused 3-sulfolene on one of the pyrroles acts as a porphodimethylidene precusor which can be used for a variety of Diels-Alder cycloaddition reactions.

A simple and flexible synthesis of pyrroles from α,β-unsaturated sulfones

Abel, Yvonne,Haake, Elmar,Haake, Gerold,Schmidt, Wolfgang,Struve, Daria,Walter, Andreas,Montforts, Franz-Peter

, p. 1978 - 1996 (2007/10/03)

The addition of alkyl isocyanoacetates and isocyanoacetonitrile to α,β-unsaturated sulfones affords a convenient and broad access to pyrroles with unusual substitution patterns (see Scheme 2). The α,β-unsaturated sulfones required as starting materials ar

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