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69673-99-0

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69673-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69673-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,7 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69673-99:
(7*6)+(6*9)+(5*6)+(4*7)+(3*3)+(2*9)+(1*9)=190
190 % 10 = 0
So 69673-99-0 is a valid CAS Registry Number.

69673-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-bis(4-aminophenyl)urea

1.2 Other means of identification

Product number -
Other names N,N'-Bis-(4-brom-benzoyl)-hydrazin

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:69673-99-0 SDS

69673-99-0Relevant articles and documents

Highly potent, broadly active antifungal agents for the treatment of invasive fungal infections

Baugh, Simon D.P.,Chaly, Anna,Weaver, Damian G.,Pelletier, Jeffrey C.,Thanna, Sandeep,Freeman, Katie B.,Reitz, Allen B.,Scott, Richard W.

, (2021)

Invasive fungal infections have become an important healthcare issue due in large part to high mortality rates under standard of care (SOC) therapies creating an urgent need for new and effective anti-fungal agents. We have developed a series of non-pepti

Compounds comprising benzophenone group, Organic electronic device comprising organic layers comprising the photo-cured of the monomer compounds

-

Paragraph 0377-0381, (2021/03/09)

The compound represented by Formula I or II is provided as an organic material layer material of an organic electronic device. The benzophenone functional group-containing compound represented by the following Chemical I or Chemical Formula II: I (Chemical Formula Ar -) (R). 1 -R2 -Bpm In the formula, m is 1 and 10, and Ar is a substituted or unsubstituted m having a C-order linking group. 6 -C60 Substituted or unsubstituted m having aryl group, C nd-linking group3 -C60 Substituted or unsubstituted fused m with heteroaryl groups or C primary linking groups6 -C60 Aryl group, R1 And R2 Each independently represents a simple bond, O - a substituted or unsubstituted C. 6 -C30 Arylene group, substituted or unsubstituted C3 -C30 Heteroarylene group, substituted or unsubstituted C1 -C10 The alkylene group and Bp are 1 divalent linking groups derived from benzophenone functional groups. Chemical Formula II. In the formula, n is at least 1 and Ar ' is a substituted or unsubstituted m having a C-order linking group. 6 -C60 Aryl group Substituted or unsubstituted m having a C nd order linker3 -C60 Substituted or unsubstituted fused m with heteroaryl groups or C primary linking groups6 -C60 Aryl group, R3 And R4 Each independently represents a simple bond, O - a substituted or unsubstituted C. 6 -C30 Arylene group, substituted or unsubstituted C3 -C30 Heteroarylene group, substituted or unsubstituted C6 -C30 Fused arylene groups, substituted or unsubstituted C1 -C10 The alkylene group and Bp ' are 1 divalent linking groups derived from benzophenone functional groups.

Fluorescent probes and application thereof to detection of neurotoxic agents

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Paragraph 0038-0041, (2020/05/01)

The invention relates to fluorescent probes represented by a general formula I or II which is described in the specification, and application of the fluorescent probes in detection of neurotoxic agents. The fluorescent probes can be used for efficiently d

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