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138377-66-9

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138377-66-9 Usage

General Description

HC Yellow No. 15 is a synthetic organic dye commonly used in the textile industry to color various materials, such as fabrics and yarn. This chemical compound belongs to the class of azo dyes, which are characterized by a specific chemical structure containing one or more nitrogen atoms connected by double bonds. HC Yellow No. 15 is known for its vibrant yellow hues and high color fastness properties, making it a popular choice for achieving bright and long-lasting coloration in textiles. However,

Check Digit Verification of cas no

The CAS Registry Mumber 138377-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,7 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 138377-66:
(8*1)+(7*3)+(6*8)+(5*3)+(4*7)+(3*7)+(2*6)+(1*6)=159
159 % 10 = 9
So 138377-66-9 is a valid CAS Registry Number.

138377-66-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-hydroxyethylamino)-3-nitrobenzamide

1.2 Other means of identification

Product number -
Other names 4-[(2-hydroxyethyl)amino]-3-nitrobenzamide

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:138377-66-9 SDS

138377-66-9Downstream Products

138377-66-9Relevant articles and documents

Novel JAK1-selective benzimidazole inhibitors with enhanced membrane permeability

Kim, Hyungmi,Kim, Mi Kyoung,Choo, Hyunah,Chong, Youhoon

supporting information, p. 3213 - 3215 (2016/07/12)

The previously identified Janus kinase 1 (JAK1)-selective inhibitor, 1-(2-aminoethyl)-2-(piperidin-4-yl)-1H-benzo[d]imidazole-5-carboxamide (2), suffered from low cell permeability, which resulted in poor pharmacokinetic properties. In this study, by introducing less polar hydrogen bond donors at N1(a hydroxyalkyl or a methylaminoalkyl group) and C2 (a cyclohexanol group) positions, a series of novel benzimidazole derivatives were prepared, which exhibited selective JAK1 inhibitory activity (IC50against JAK1?=?0.08–0.15?μM; JAK1-selectivity?=?26–40 fold vs JAK2, 12–23 fold vs JAK3, and 38–54 fold vs Tyk2) along with significantly increased lipophilicity (3.3–15.8 times) as well as membrane permeability (6.3–12 times).

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