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135-13-7

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135-13-7 Usage

Synthesis Reference(s)

Tetrahedron Letters, 27, p. 4625, 1986 DOI: 10.1016/S0040-4039(00)85022-4

Check Digit Verification of cas no

The CAS Registry Mumber 135-13-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 135-13:
(5*1)+(4*3)+(3*5)+(2*1)+(1*3)=37
37 % 10 = 7
So 135-13-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H8O4S/c10-8(11)5-14-7-4-2-1-3-6(7)9(12)13/h1-4H,5H2,(H,10,11)(H,12,13)/p-2

135-13-7 Well-known Company Product Price

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  • Alfa Aesar

  • (A12705)  2-(Carboxymethylthio)benzoic acid, 97%   

  • 135-13-7

  • 1g

  • 545.0CNY

  • Detail
  • Alfa Aesar

  • (A12705)  2-(Carboxymethylthio)benzoic acid, 97%   

  • 135-13-7

  • 5g

  • 1972.0CNY

  • Detail

135-13-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(carboxymethylsulfanyl)benzoic acid

1.2 Other means of identification

Product number -
Other names o-Carboxyphenylthioglycollic acid

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:135-13-7 SDS

135-13-7Relevant articles and documents

Emission Control of a Pyrene-thioindigo Compound

Saika, Tetsuyuki,Iyoda, Tomokazu,Honda, Kenichi,Shimidzu, Takeo

, p. 591 - 592 (1992)

Two distinct fluorescence modes of a thioindigo compound substituted with two pyrene groups on the 7 and 7' positions were controlled by geometrical photoisomerization of the thioindigo skeleton.

SUBSTITUTED DIHYDROINDENE-4-CARBOXAMIDES AND ANALOGS THEREOF, AND METHODS USING SAME

-

Page/Page column 232, (2018/10/19)

The present invention includes novel substituted bicyclic compounds, and compositions comprising the same, that can be used to treat or prevent hepatitis B virus (HBV) infections in a patient. In certain embodiments, the compounds and compositions of the invention are capsid inhibitors. (Formula I)

An unexpected triethylsilane-triggered rearrangement of thioaurones to thioflavonols under SPPS conditions

Varedian, Miranda,Langer, Vratislav,Bergquist, Jonas,Gogoll, Adolf

supporting information; experimental part, p. 6033 - 6035 (2009/04/11)

Thioaurones are converted to a mixture of thiaindenes and thioflavonols when exposed to reaction conditions employed in SPPS, that is, treatment with trifluoroacetic acid in the presence of triethylsilane.

Metallation reactions. Part 35: A change of the regiochemistry in the metallation of (alkylthio)arenes

Cabiddu, Maria G.,Cabiddu, Salvatore,Cadoni, Enzo,De Montis, Stefania,Fattuoni, Claudia,Melis, Stefana

, p. 3915 - 3920 (2007/10/03)

The metallation reaction of bromo(alkylthio)benzenes is described. The results show the complementarity of these reactions with the metal-hydrogen exchange reaction. In fact, monometallation of bromo(methylthio)benzenes afforded products substituted in para or meta or ortho to the thioethereal function while bimetallation led to αS,para, αS,meta and αS,ortho disubstituted products. Analogously, the monometallation of 4-bromo-(isopropylthio)benzene afforded para-monosubstituted and ortho,para-disubstituted products.

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