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2492-26-4

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2492-26-4 Usage

Uses

Different sources of media describe the Uses of 2492-26-4 differently. You can refer to the following data:
1. copper corrosion inhibitor; plasticizer and photometer for acid copper plating.
2. sodium mercaptobenzothiazole solution, also known as sodium mbt50%, or simply mbt50, is a clear, amber 50% aqueous solution of sodium 2-mercaptobenzothiazole represented by the formula: (nac7h4ns2). mbt50 is used as a corrosion inhibitor and water treatment agent; biological activity indicates possible use as a bactericide or fungicide. it is also used as a chemical intermediate.

General Description

Sodium 2-mercaptobenzothiazol solution appears as an amber liquid with an odor of old rubber. A 50% aqueous solution. Denser than water. (USCG, 1999)

Air & Water Reactions

Sensitive to prolonged exposure to air. Water soluble.

Reactivity Profile

SODIUM 2-MERCAPTOBENZOTHIAZOL reacts vigorously with oxidizing materials (e.g. hydroperoxides). Liberates heat in contact with strong mineral acids or acid fumes .

Health Hazard

Contact with moisture in the body by inhalation may yield sodium hydroxide (corrosive) and 2-mercaptabenzothiazole, an irritant. Contact with the eyes caused opacity or ulceration of the cornea, inflammation of the iris, redness and swelling of the conjunctiva and partial eversion of the eye lids, and destruction or irreversible tissue change in 24 hours or less (rabbit). A dose of 2,500 mg/kg applied to the skin caused severe depression, cold extremities, appetite loss; 4 of 10 died. Exposure of the skin to 1,250 mg/kg caused a severe degree of skin injury. The skin was burned in 24 hours with formation of hard eschar at 1-2 weeks; 1 of 10 rabbits died. Ingestion caused tremors, convulsions, severe depression and hemaluria in male rats. Ingestion of 312.5 mg/kg: 1 of 5 male rats die on day 2; 625 mg/kg: 2 of 5 died within 3-5 minutes; 1,250 mg/kg: 3 of 5 died within 3-5 minutes; 2,500 mg/kg: 100% mortality within 3-5 minutes. Hemorrhage of the stomach occurred in all rats that died.

Safety Profile

Moderately toxic by ingestion. When heated to decomposition it emits very toxic fumes of NOx, SOx, and NazO. See also MERCAPTANS.

Regulations

Sodium 2-mercaptobenzothiazole was first registered as a pesticide in the United States in 1949 in an industrial preservative product. Currently, only one product is registered, for use in wood and paper/paperboard treatment and as a preservative in metal working cutting fluids, emulsions, textiles and pastes.sodium and zinc salts of 2-mercaptobenzothiazole

Check Digit Verification of cas no

The CAS Registry Mumber 2492-26-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,9 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2492-26:
(6*2)+(5*4)+(4*9)+(3*2)+(2*2)+(1*6)=84
84 % 10 = 4
So 2492-26-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H5NS2.Na/c9-7-8-5-3-1-2-4-6(5)10-7;/h1-4H,(H,8,9);/q;+1

2492-26-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Sodium mercaptobenzothiazole

1.2 Other means of identification

Product number -
Other names sodiumbenzothiazolethiolate

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:2492-26-4 SDS

2492-26-4Synthetic route

2-Mercaptobenzothiazole
149-30-4

2-Mercaptobenzothiazole

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

Conditions
ConditionsYield
With sodium hydroxide In water at 14.99℃; Equilibrium constant; Temperature;
bromocyane
506-68-3

bromocyane

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

benzo[d]thiazol-2-yl thiocyanate
6011-99-0

benzo[d]thiazol-2-yl thiocyanate

Conditions
ConditionsYield
Ambient temperature;100%
With water
With ethanol
With ethanol
With water
sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

cyanogen chloride
506-77-4

cyanogen chloride

benzo[d]thiazol-2-yl thiocyanate
6011-99-0

benzo[d]thiazol-2-yl thiocyanate

Conditions
ConditionsYield
Ambient temperature;100%
With water
With ethanol
With ethanol
With water
benzyl bromide
100-39-0

benzyl bromide

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

2-benzylthiobenzothiazole
19654-17-2

2-benzylthiobenzothiazole

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃;99%
2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxan-4-yl)acetic acid n-hexyl ester

2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxan-4-yl)acetic acid n-hexyl ester

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

2-((4R,6S)-6-(benzo(d)thiazol-2-ylthio)methyl-2-oxo-1,3-dioxan-4-yl)acetic acid n-hexyl ester

2-((4R,6S)-6-(benzo(d)thiazol-2-ylthio)methyl-2-oxo-1,3-dioxan-4-yl)acetic acid n-hexyl ester

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 70℃; for 6h;98.5%
2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxan-4-yl)acetic acid benzyl ester

2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxan-4-yl)acetic acid benzyl ester

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

2-((4R,6S)-6-(benzo(d)thiazol-2-ylthio)methyl-2-oxo-1,3-dioxan-4-yl)acetic acid benzyl ester

2-((4R,6S)-6-(benzo(d)thiazol-2-ylthio)methyl-2-oxo-1,3-dioxan-4-yl)acetic acid benzyl ester

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 70℃; for 6h;98.3%
2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxan-4-yl)acetic acid cyclohexyl ester

2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxan-4-yl)acetic acid cyclohexyl ester

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

2-((4R,6S)-6-(benzo(d)thiazol-2-ylthio)methyl-2-oxo-1,3-dioxan-4-yl)acetic acid cyclohexyl ester

2-((4R,6S)-6-(benzo(d)thiazol-2-ylthio)methyl-2-oxo-1,3-dioxan-4-yl)acetic acid cyclohexyl ester

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 70℃; for 6h;98.2%
sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

di(benzothiazol-2-yl)disulfide
120-78-5

di(benzothiazol-2-yl)disulfide

Conditions
ConditionsYield
With bromonitromethane In methanol98%
With water; chlorine; ammonium chloride
With sulfuric acid; water; dihydrogen peroxide
2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxane-4-yl)acetic acid tert-butyl ester

2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxane-4-yl)acetic acid tert-butyl ester

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

2-((4R,6S)-6-(benzo(d)thiazol-2-ylthio)methyl-2-oxo-1,3-dioxan-4-yl)acetic acid tert-butyl ester

2-((4R,6S)-6-(benzo(d)thiazol-2-ylthio)methyl-2-oxo-1,3-dioxan-4-yl)acetic acid tert-butyl ester

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 70℃; for 6h; Solvent; Temperature;98%
3-bromo-1-(trimethylsilyl)-1-propyne
38002-45-8

3-bromo-1-(trimethylsilyl)-1-propyne

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

2-[3-(trimethylsilyl)prop-2-ynylthio]benzo[d]thiazole
504440-54-4

2-[3-(trimethylsilyl)prop-2-ynylthio]benzo[d]thiazole

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃; for 5h;97%
In N,N-dimethyl-formamide at 20℃;97%
2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxan-4-yl)acetic acid methyl ester

2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxan-4-yl)acetic acid methyl ester

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

2-((4R,6S)-6-(benzo(d)thiazol-2-ylthio)methyl-2-oxo-1,3-dioxan-4-yl)acetic acid methyl ester

2-((4R,6S)-6-(benzo(d)thiazol-2-ylthio)methyl-2-oxo-1,3-dioxan-4-yl)acetic acid methyl ester

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 70℃; for 6h;97%
2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxan-4-yl)acetic acid ethyl ester

2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxan-4-yl)acetic acid ethyl ester

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

2-((4R,6S)-6-(benzo(d)thiazol-2-ylthio)methyl-2-oxo-1,3-dioxan-4-yl)acetic acid ethyl ester

2-((4R,6S)-6-(benzo(d)thiazol-2-ylthio)methyl-2-oxo-1,3-dioxan-4-yl)acetic acid ethyl ester

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 70℃; for 6h;97%
2-((4R,6S)-6-chloromethyl-2-oxo-1,3-dioxan-4-yl)acetic acid tert-butyl ester

2-((4R,6S)-6-chloromethyl-2-oxo-1,3-dioxan-4-yl)acetic acid tert-butyl ester

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

2-((4R,6S)-6-(benzo(d)thiazol-2-ylthio)methyl-2-oxo-1,3-dioxan-4-yl)acetic acid tert-butyl ester

2-((4R,6S)-6-(benzo(d)thiazol-2-ylthio)methyl-2-oxo-1,3-dioxan-4-yl)acetic acid tert-butyl ester

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 70℃; for 6h;96%
2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxane-4-yl)acetic acid tert-butyl ester

2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxane-4-yl)acetic acid tert-butyl ester

acetone
67-64-1

acetone

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

(4R,6S)-6-(benzothiazol-2-mercapto)methyl-2,2-dimethyl-1,3-dioxane-4-acetic acid tert-butyl ester
1353750-24-9

(4R,6S)-6-(benzothiazol-2-mercapto)methyl-2,2-dimethyl-1,3-dioxane-4-acetic acid tert-butyl ester

Conditions
ConditionsYield
Stage #1: 2-((4R,6S)-6-bromomethyl-2-oxo-1,3-dioxane-4-yl)acetic acid tert-butyl ester; acetone; sodium 2-mercaptobenzothiazole at 60℃; for 6h;
Stage #2: With toluene-4-sulfonic acid at 20℃; for 5h;
95.8%
cyclohexylamine
108-91-8

cyclohexylamine

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

N-(cyclohexyl)benzothiazole-2-sulfenamide
95-33-0

N-(cyclohexyl)benzothiazole-2-sulfenamide

Conditions
ConditionsYield
Stage #1: cyclohexylamine; sodium 2-mercaptobenzothiazole With sulfuric acid; dihydrogen peroxide In water at 40 - 45℃; for 3 - 5h; Alkaline conditions;
Stage #2: With sodium hypochlorite In water for 0.166667 - 0.633333h;
95.2%
With sulfuric acid; dihydrogen peroxide In water at 50℃; for 2h; Conversion of starting material;84%
With alkaline aqueous solution; chloro-air mixture
sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

[4R,6R,6(1R)]-4-allyl-6-[1-methyl-2-(methanesulfonyl)ethyl]-4H-pyran-2-one
237735-32-9

[4R,6R,6(1R)]-4-allyl-6-[1-methyl-2-(methanesulfonyl)ethyl]-4H-pyran-2-one

(4R,6R)-4-Allyl-6-[(S)-2-(benzothiazol-2-ylsulfanyl)-1-methyl-ethyl]-tetrahydro-pyran-2-one
237735-47-6

(4R,6R)-4-Allyl-6-[(S)-2-(benzothiazol-2-ylsulfanyl)-1-methyl-ethyl]-tetrahydro-pyran-2-one

Conditions
ConditionsYield
94%
2-thenyl bromide
45438-73-1

2-thenyl bromide

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

2-((thiophen-2-ylmethyl)thio)benzo[d]thiazole
189579-62-2

2-((thiophen-2-ylmethyl)thio)benzo[d]thiazole

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃;94%
N-(p-Toluensulfonyl)iminothiokohlensaeuremethylester-chlorid
2973-83-3

N-(p-Toluensulfonyl)iminothiokohlensaeuremethylester-chlorid

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

N-[1-(Benzothiazol-2-ylsulfanyl)-1-methylsulfanyl-meth-(E)-ylidene]-4-methyl-benzenesulfonamide
93488-25-6

N-[1-(Benzothiazol-2-ylsulfanyl)-1-methylsulfanyl-meth-(E)-ylidene]-4-methyl-benzenesulfonamide

Conditions
ConditionsYield
In benzene for 4h; Heating;92%
1-bromomethyl-4-nitro-benzene
100-11-8

1-bromomethyl-4-nitro-benzene

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

2-((4-nitrobenzyl)thio)benzo[d]thiazole
92905-87-8

2-((4-nitrobenzyl)thio)benzo[d]thiazole

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃;91%
9-bromomethylphenantrene
24471-57-6

9-bromomethylphenantrene

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

2-[(phenanthren-9-ylmethyl)thio]benzo[d]thiazole

2-[(phenanthren-9-ylmethyl)thio]benzo[d]thiazole

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃; for 6h;91%
sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

Methanesulfonic acid (R)-2-((2R,4R)-4-allyl-6-methoxy-tetrahydro-pyran-2-yl)-propyl ester

Methanesulfonic acid (R)-2-((2R,4R)-4-allyl-6-methoxy-tetrahydro-pyran-2-yl)-propyl ester

2-[(S)-2-((2R,4R)-4-Allyl-6-methoxy-tetrahydro-pyran-2-yl)-propylsulfanyl]-benzothiazole
544429-69-8

2-[(S)-2-((2R,4R)-4-Allyl-6-methoxy-tetrahydro-pyran-2-yl)-propylsulfanyl]-benzothiazole

Conditions
ConditionsYield
90%
2-bromo-2-nitropropane
5447-97-2

2-bromo-2-nitropropane

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

1,3-benzothiazol-2-yl 1-methyl-1-nitroethyl sulphide
75376-74-8

1,3-benzothiazol-2-yl 1-methyl-1-nitroethyl sulphide

Conditions
ConditionsYield
In N,N-dimethyl-formamide Irradiation;89%
In N,N-dimethyl-formamide for 1h; Irradiation;89%
sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

cyanomethyl bromide
590-17-0

cyanomethyl bromide

(1,3-benzothiazol-2-ylsulfanyl)acetonitrile
24793-01-9

(1,3-benzothiazol-2-ylsulfanyl)acetonitrile

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃; for 3h;89%
4,5-dibromo-2-furfurylidenemalononitrile
93362-26-6

4,5-dibromo-2-furfurylidenemalononitrile

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

2-[5-(Benzothiazol-2-ylsulfanyl)-4-bromo-furan-2-ylmethylene]-malononitrile
93362-35-7

2-[5-(Benzothiazol-2-ylsulfanyl)-4-bromo-furan-2-ylmethylene]-malononitrile

Conditions
ConditionsYield
3-6h on a steam bath;88.6%
ethyl bromofluoroacetate
401-55-8

ethyl bromofluoroacetate

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

ethyl 2-(benzothiazol-2-ylsulfanyl)-2-fluoroacetate

ethyl 2-(benzothiazol-2-ylsulfanyl)-2-fluoroacetate

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃; for 1h;88%
In N,N-dimethyl-formamide at 20℃; for 1h;82%
In N,N-dimethyl-formamide at 40℃; for 1.5h;
4,5-dibromo-2-furfurylidenecyanoacetate
93362-27-7

4,5-dibromo-2-furfurylidenecyanoacetate

sodium 2-mercaptobenzothiazole
2492-26-4

sodium 2-mercaptobenzothiazole

(E)-3-[5-(Benzothiazol-2-ylsulfanyl)-4-bromo-furan-2-yl]-2-cyano-acrylic acid methyl ester
93362-30-2

(E)-3-[5-(Benzothiazol-2-ylsulfanyl)-4-bromo-furan-2-yl]-2-cyano-acrylic acid methyl ester

Conditions
ConditionsYield
3-6h on a steam bath;87.5%

2492-26-4Upstream product

2492-26-4Relevant articles and documents

A chemical looping technology for the synthesis of 2,2′-dibenzothiazole disulfide

Tian, Jiaxin,Jiayu Hu,Wang, Kai,Deng, Jian,Luo, Guangsheng

, p. 2778 - 2785 (2020/06/17)

A novel chemical looping technology for the synthesis of 2,2′-dibenzothiazole disulfide (MBTS) with zero emissions has been developed. Through chemical cycling between carbonate and bicarbonate in the reaction system, the insoluble 2-mercaptobenzothiazole (MBT) can become soluble in the aqueous phase of sodium carbonate and then be oxidized efficiently by hydrogen peroxide and the absorption of CO2 with high selectivity. The mother liquor can be totally recycled by the desorption of CO2 without any generation of salt-containing wastewater. With the new synthesis technology, the product has high purity and reaches the standard of a superior product that can be applied as a vulcanization accelerator. When 5.0 wt% hydrogen peroxide was added dropwise over 40 min at 50 °C, the conversion ratio of MBT was over 98%. The mother liquor was recycled 5 times and no side-products were found. The whole process is clean and pollution-free, which greatly reduces the burden of hazardous waste treatment and brings great environmental benefits.

NOVEL METHOD FOR PREPARING ROSUVASTATIN, INTERMEDIATE COMPOUNDS USEFUL FOR PREPARING SAME, AND METHOD FOR PREPARING SAME

-

Page/Page column 10, (2012/06/16)

The present invention relates to novel intermediate compounds used in preparing Rosuvastatin or the pharmaceutically acceptable salts thereof, to a method for preparing same, and to a method for preparing Rosuvastatin or the pharmaceutically acceptable salts thereof from the intermediates. The preparation method of the present invention has the effect of providing Rosuvastatin hemi-calcium salts with an excellent yield rate.

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