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151915-07-0

Benzenesulfonamide, N-ethyl-2,4,6-trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 151915-07-0 Structure

  • Basic information

    1. Product Name: Benzenesulfonamide, N-ethyl-2,4,6-trimethyl-
    2. Synonyms:
    3. CAS NO:151915-07-0
    4. Molecular Formula: C11H17NO2S
    5. Molecular Weight: 227.327
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 151915-07-0.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: Benzenesulfonamide, N-ethyl-2,4,6-trimethyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenesulfonamide, N-ethyl-2,4,6-trimethyl-(151915-07-0)
    11. EPA Substance Registry System: Benzenesulfonamide, N-ethyl-2,4,6-trimethyl-(151915-07-0)

  • 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: 151915-07-0(Hazardous Substances Data)

151915-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151915-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,9,1 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 151915-07:
(8*1)+(7*5)+(6*1)+(5*9)+(4*1)+(3*5)+(2*0)+(1*7)=120
120 % 10 = 0
So 151915-07-0 is a valid CAS Registry Number.

151915-07-0SDS

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 N-ethyl-2,4,6-trimethylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names 2,4,6-trimethyl-benzenesulfonic acid ethylamide

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:151915-07-0 SDS

151915-07-0Relevant articles and documents

Synthesis and evaluation of unsymmetrical polyamine derivatives as antitumor agents

Wang, Jianhong,Xie, Songqiang,Li, Yanjie,Guo, Yongjun,Ma, Yuanfang,Zhao, Jin,Phanstiel IV, Otto,Wang, Chaojie

, p. 7005 - 7012 (2008/12/22)

A series of unsymmetrically substituted polyamine derivatives were prepared and their cytotoxicities in mouse leukemia L1210, melanoma B16, and HeLa cells were investigated. The in vitro cytotoxicity revealed that these conjugates could recognize the poly

AMINO THIOL COMPOUNDS AND COMPOSITIONS FOR USE IN CONJUNCTION WITH CANCER THERAPY

-

Page/Page column 56-57, (2010/02/10)

The invention provides novel polyamine and amino thiol compounds and pharmaceutical compositions for administration in conjunction with cancer chemotherapy or radiation therapy. The compounds are administered locally to provide protection against the adve

The synthesis of N(I),N(II)-diethyl[6-14C]norspermine ([14C]Cl-1006), a new anticancer drug

Hicks, James L.,Huang, Yun

, p. 275 - 284 (2007/10/03)

N(I),N(II)-Diethylnorspermine, CI-1006, a potential new anticancer drug, was synthesized with a carbon-14 located at the central carbon of the molecule. Condensation of N-(2,4,6-trimethylbenzenesulfonyl)-N-ethylpropane-1,3-diamine with diethy[2-14/s

Synthesis and evaluation of unsymmetrically substituted polyamine analogues as modulators of human spermidine/spermine-N1-acetyltransferase (SSAT) and as potential antitumor agents

Saab,West,Bieszk,Preuss,Mank,Casero Jr.,Woster

, p. 2998 - 3004 (2007/10/02)

Spermidine/spermine-N1-acetyltranferase (SSAT), the rate-limiting step in polyamine catabolism, is critical for the interconversion and modulation of cellular polyamines. Inhibitor-initiated induction of this enzyme also appears to correlate wi

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