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Cyclobutanecarboxylic acid, 1-formyl-, methyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 155380-49-7 Structure
  • Basic information

    1. Product Name: Cyclobutanecarboxylic acid, 1-formyl-, methyl ester (9CI)
    2. Synonyms: Cyclobutanecarboxylic acid, 1-formyl-, methyl ester (9CI)
    3. CAS NO:155380-49-7
    4. Molecular Formula: C7H10O3
    5. Molecular Weight: 142.1525
    6. EINECS: N/A
    7. Product Categories: CARBOXYLICESTER;ALDEHYDE
    8. Mol File: 155380-49-7.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: Cyclobutanecarboxylic acid, 1-formyl-, methyl ester (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclobutanecarboxylic acid, 1-formyl-, methyl ester (9CI)(155380-49-7)
    11. EPA Substance Registry System: Cyclobutanecarboxylic acid, 1-formyl-, methyl ester (9CI)(155380-49-7)
  • 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: 155380-49-7(Hazardous Substances Data)

155380-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155380-49-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,3,8 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 155380-49:
(8*1)+(7*5)+(6*5)+(5*3)+(4*8)+(3*0)+(2*4)+(1*9)=137
137 % 10 = 7
So 155380-49-7 is a valid CAS Registry Number.

155380-49-7SDS

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 1-Formyl-1-methylcyclobutanecarboxylate

1.2 Other means of identification

Product number -
Other names methyl 1-formylcyclobutanecarboxylate

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:155380-49-7 SDS

155380-49-7Downstream Products

155380-49-7Relevant articles and documents

CYCLOPROPYLAMINES AS LSD1 INHIBITORS

-

Paragraph 0509; 0510, (2015/09/22)

The present invention is directed to cyclopropylamine derivatives which are LSD1 inhibitors useful in the treatment of diseases such as cancer.

ANDROGEN RECEPTOR ANTAGONISTS AND USES THEREOF

-

Page/Page column 117, (2012/09/22)

Disclosed are substituted thioimidazolidinone compounds and pharmaceutical compositions comprising such compounds. The compounds and compositions can be used for treatment of androgen receptor-associated diseases or disorders, such as prostate cancer, benign prostatic hypertrophy, male hair loss and hypertrichosis.

SUBSTITUTED ARYLPYRAZOLES

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Page/Page column 73, (2010/11/25)

This invention relates to a range of C4 substituted aryl pyrazoles of Formula (I) including those 1-arylpyrazoles in which the 4-position is substituted with an acyclic substituent, a cycloalkyl ring structure or heterocyclic ring structure and which comp

Tetramethyl 1,1,4,4-Cyclohexanetetracarboxylate: Preparation and Conversion to Key Precursors of Fluorinated, Stereochemically Defined Cyclohexanes

Davis, Charles R.,Swenson, Dale C.,Burton, Donald J.

, p. 6843 - 6850 (2007/10/02)

Stereoselective low-temperature diisobutylaluminum hydride (DIBALH) reduction of the litle tetraester 3 affords trans-1,4-dialdehyde 4a as the major product.Fluorination of 4a,b, followed by additional elaboration leads to novel, 1,1,4,4-tetrasubstituted cyclohexanes bearing trans-1,4-difluoromethyl and fluoromethyl groups.The effect of ring size and number of ester substituents on the outcome of the reduction has been examined and treatment of dimethyl 1,1-cycloalkyl diesters 7a-c with excess DIBALH results in reduction of only one ester group.An entry into trans-1,4-trifluoromethylated tetrasubstituted cyclohexanes has been gained through stereoselective SF4 fluorination of 1,1,4,4-cyclohexanetetracarboxylic acid 17.Stereochemical assignments are supported by X-ray crystallographic data.

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