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91914-26-0

Benzoic acid, 4-[5,6-dihydro-4-(4-methoxy-3-sulfophenyl)benzo[h]quinolin-2-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91914-26-0

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91914-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91914-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,1 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91914-26:
(7*9)+(6*1)+(5*9)+(4*1)+(3*4)+(2*2)+(1*6)=140
140 % 10 = 0
So 91914-26-0 is a valid CAS Registry Number.

91914-26-0SDS

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 4-[4-(4-Methoxy-3-sulfo-phenyl)-5,6-dihydro-benzo[h]quinolin-2-yl]-benzoic acid

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:91914-26-0 SDS

91914-26-0Downstream Products

91914-26-0Relevant articles and documents

PYRYLIUM-MEDIATED TRANSFORMATIONS OF NATURAL PRODUCTS. PART 7. DISPLACEMENT OF THE N-SUBSTITUENTS OF PYRIDINIUM IONS IN AQUEOUS SOLUTION: REPLACEMENT OF THE ω-AMINO GROUP OF LYSINE, AND OF THE TERMINAL AMINO GROUP OF GLYCYLGLYCINE

Katritzky, Alan R.,Yang, Yu-Kun

, p. 885 - 890 (2007/10/02)

In two-step sequences, lysine has been converted into the thio-substituted derivatives RS4CH(NH2)CO2H (R=Ph or PhCH2), and glycylglycine into PhSCH2CONHCH2CO2H.All reactions proceeded in aqueous solution at /= 75 deg C; they thus provide models for the selective conversion of proteins at the ω-amino groups of lysine side chains and at the terminal amino groups, respectively.

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