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CHEMBRDG-BB 4022329 is a chemical compound characterized by the molecular formula C22H13N3O4S2. It is a benzothiazole derivative known for its potential applications in pharmaceuticals and agrochemicals. CHEMBRDG-BB 4022329 may exhibit antioxidant and antimicrobial properties, which could be instrumental in the development of innovative drugs and agricultural products. However, comprehensive research is still required to fully explore its capabilities and applications.

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  • 16183-32-7 Structure
  • Basic information

    1. Product Name: CHEMBRDG-BB 4022329
    2. Synonyms: CHEMBRDG-BB 4022329;AKOS LT-992X0028;N-(4-CHLOROBENZYL)BUTAN-1-AMINE;N-(4-CHLOROPHENYLMETHYL)BUTYLAMINE;UKRORGSYN-BB BBV-125481;2298-58-0 (Hydrochloride);Aids107180;Aids-107180
    3. CAS NO:16183-32-7
    4. Molecular Formula: C11H16ClN
    5. Molecular Weight: 197.707
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16183-32-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 264.2°Cat760mmHg
    3. Flash Point: 113.6°C
    4. Appearance: /
    5. Density: 1.026g/cm3
    6. Vapor Pressure: 0.00984mmHg at 25°C
    7. Refractive Index: 1.516
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: CHEMBRDG-BB 4022329(CAS DataBase Reference)
    11. NIST Chemistry Reference: CHEMBRDG-BB 4022329(16183-32-7)
    12. EPA Substance Registry System: CHEMBRDG-BB 4022329(16183-32-7)
  • 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: 16183-32-7(Hazardous Substances Data)

16183-32-7 Usage

Uses

Used in Pharmaceutical Industry:
CHEMBRDG-BB 4022329 is used as a potential active pharmaceutical ingredient for its possible antioxidant and antimicrobial properties. These characteristics make it a candidate for the development of new drugs that could address various health conditions, including infections and diseases associated with oxidative stress.
Used in Agrochemical Industry:
In the agrochemical sector, CHEMBRDG-BB 4022329 is utilized as a component in the formulation of products with antimicrobial properties. Its potential to combat microbial infections in crops can contribute to the enhancement of agricultural yields and the development of more effective pest and disease control strategies.
Further research is essential to determine the specific applications and optimal use of CHEMBRDG-BB 4022329 in these industries, ensuring its safety and efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 16183-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,8 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16183-32:
(7*1)+(6*6)+(5*1)+(4*8)+(3*3)+(2*3)+(1*2)=97
97 % 10 = 7
So 16183-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H16ClN/c1-2-3-8-13-9-10-4-6-11(12)7-5-10/h4-7,13H,2-3,8-9H2,1H3

16183-32-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(4-chlorophenyl)methyl]butan-1-amine

1.2 Other means of identification

Product number -
Other names Benzenemethanamine,N-butyl-4-chloro

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:16183-32-7 SDS

16183-32-7Downstream Products

16183-32-7Relevant articles and documents

Single source precursor synthesized CuS nanoparticles for NIR phototherapy of cancer and photodegradation of organic carcinogen

Arshad, Mehwish,Wang, Zhaojie,Nasir, Jamal Abdul,Amador, Eric,Jin, Mingwu,Li, Haibin,Chen, Zhigang,Rehman, Zia ur,Chen, Wei

, (2021)

Herein, we report cost effective and body compatible CuS nanoparticles (NPs) derived from a single source precursor as photothermal agent for healing deep cancer and photocatalytic remediation of organic carcinogens. These NPs efficiently kill MCF7 cells

Rhodium catalysts with cofactor mimics for the biomimetic reduction of CN bonds

Chen, Fushan,Deng, Li,Dong, Wenjin,Tang, Jie,Xian, Mo

, p. 5564 - 5569 (2021/08/25)

A strategy based on the cooperation between metal and bonded cofactor mimics was applied to the transfer hydrogenation of CN bonds. We designed and synthesized a rhodium complex containing a 1,3-dimethylbenzoimidazole moiety, which could transfer hydride from a rhodium center to imine substrates in a biomimetic way. Under both transfer hydrogenation and reductive amination reaction conditions, the catalyst exhibited good selectivity towards CN bonds. With the catalyst, 34 imines were transfer hydrogenated to corresponding amines and a key intermediate of retigabine was prepared via reductive amination in a greener way. According to the NMR observations and isotope experiments, a plausible mechanism for this biomimetic reduction of CN bonds were proposed.

Polyoxometalate-Driven Ease Conversion of Valuable Furfural to trans- N, N-4,5-Diaminocyclopenten-2-ones

Fountoulaki, Stella,Lykakis, Ioannis N.,Tzani, Marina A.

, (2022/02/10)

We investigated the catalytic efficacy of silicotungstic acid (H4SiW12O40) polyoxometalate (POM) toward the reaction between furfural and amines that selectively yields trans-N,N-4,5-substituted-diaminocyclopenten-2-ones (trans-DACPs). H4SiW12O40 facilita

Bio-inspired transition metal-organic hydride conjugates for catalysis of transfer hydrogenation: Experiment and theory

McSkimming, Alex,Chan, Bun,Bhadbhade, Mohan M.,Ball, Graham E.,Colbran, Stephen B.

, p. 2821 - 2834 (2015/02/05)

Taking inspiration from yeast alcohol dehydrogenase (yADH), a benzimidazolium (BI+) organic hydride-acceptor domain has been coupled with a 1,10-phenanthroline (phen) metal-binding domain to afford a novel multifunctional ligand (LBI+/sup

Bio-inspired catalytic imine reduction by rhodium complexes with tethered hantzsch pyridinium groups: Evidence for direct hydride transfer from dihydropyridine to metal-activated substrate

McSkimming, Alex,Bhadbhade, Mohan M.,Colbran, Stephen B.

supporting information, p. 3411 - 3416 (2013/05/08)

Inspired by Nature: A conceptually new design for a catalyst, combining a metal center abutted to an organic hydride donor, is demonstrated for the formate-driven transfer hydrogenation of imines under ambient conditions. A key step, transfer of hydride from the organohydride donor to the metal-polarized substrate, mirrors that in metallo-(de)hydrogenase enzymes.

SUBSTITUTED SULFONAMIDES USEFUL AS ANTIAPOPTOTIC BCL INHIBITORS

-

Page/Page column 216, (2012/12/13)

Disclosed are compounds of Formula (I), or a pharmaceutically acceptable salt thereof, wherein: W and Q and G are defined herein. Also disclosed are methods of using such compounds as inhibitors of Bcl-2 family antiapoptotic proteins for the treatment of cancer; and pharmaceutical compositions comprising such compounds.

1,2,3-Triazole-boranes: Stable and efficient reagents for ketone and aldehyde reductive amination in organic solvents or in water

Liao, Wenyan,Chen, Yunfeng,Liu, Yuxiu,Duan, Haifeng,Petersen, Jeffrey L.,Shi, Xiaodong

supporting information; experimental part, p. 6436 - 6438 (2010/03/04)

Air, moisture and thermally stable 1,2,3-triazole-borane complexes were developed as new practical reagents for ketone/aldehyde amination with high efficiency and excellent substrate diversity.

Sodium borohydride-iodine, an efficient reagent for reductive amination of aromatic aldehydes

Saxena, Ira,Borah, Ruli,Sarma, Jadab C.

, p. 1970 - 1971 (2007/10/03)

Reactions of aromatic aldehydes with primary amines give the corresponding secondary amines in the presence of iodine and sodium borohydride in methanol.

Reductive amination of aromatic aldehydes and ketones with nickel boride

Saxena, Ira,Borah, Ruli,Sarma, Jadab C.

, p. 503 - 504 (2007/10/03)

The reductive amination of aromatic aldehydes and ketones with nickel boride was investigated. The reactions of aromatic aldehydes and ketones with primary amines produced corresponding secondary amines in the presence of in situ generated nickel boride. The secondary amines were found to remain inert in the system.

Composition for treating depression with (N-heteroaryl)alkylamines

-

, (2008/06/13)

The invention concerns compounds having formula: STR1 or a salt thereof, wherein E represents hydrogen, lower alkyl or a group Ar 1 --A 1 --; Ar and Ar 1 are the same or different aryl groups (including heteroaryl) which are optionally substituted, eg by one or more substituents commonly used in pharmaceutical chemistry; A and A 1 are the same or different alkylene groups having one or two carbon atoms linking Ar or Ar 1 to N and optionally substituted by lower alkyl and/or optionally substituted aryl, B is an alkylene group of 3 or 4 carbon atoms, which may be substituted by lower alkyl; D 1 represents halogen, CH 3, CR 1 R 2 NH 2, SO 3 H or SO 2 NR 6 R 7 where R 1 and R 2 are independently hydrogen or lower alkyl and R 6 and R 7 are each hydrogen, lower alkyl or aralkyl of 7 to 12 carbon atoms or R 6 and R 7 together with the nitrogen atom to which they are attached represent a 5 or 6 membered ring, which compounds are useful, for treating depression or cerebral insufficiency or dementias in animals.

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